Canonical Allele Identifier: CA009289
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 201004
ClinVar RCV Id: RCV000182444
dbSNP Id: rs794728646

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64804452_64804457del , CM000673.2:g.64804452_64804457del GRCh38
NC_000011.9:g.64571924_64571929del , CM000673.1:g.64571924_64571929del GRCh37
NC_000011.8:g.64328500_64328505del NCBI36
NG_008929.1:g.11838_11843del , LRG_509:g.11838_11843del
NG_033040.1:g.3785_3790del

Transcript Alleles

HGVS Amino-acid change
ENST00000377313.7:c.1725_1730del ENSP00000366530.1:p.Ile575_Ser577delinsMet
ENST00000394374.8:c.*1018_*1023del ENSP00000377899.4:n.*1018_*1023del
ENST00000394376.7:c.1701_1706del ENSP00000377901.3:p.Ile567_Ser569delinsMet
ENST00000413626.2:c.1710_1715del ENSP00000411218.2:p.Ile570_Ser572delinsMet
ENST00000424912.2:c.1710_1715del ENSP00000388016.2:p.Ile570_Ser572delinsMet
ENST00000429702.6:c.1710_1715del ENSP00000402752.2:p.Ile570_Ser572delinsMet
ENST00000672079.2:c.*806_*811del ENSP00000500905.2:n.*806_*811del
ENST00000710881.1:c.1725_1730del ENSP00000518530.1:p.Ile575_Ser577delinsMet
ENST00000394376.6:c.1052_1057del
ENST00000478548.3:n.2203_2208del
ENST00000671939.2:n.1672_1677del
ENST00000312049.11:c.1710_1715del ENSP00000308975.6:p.Ile570_Ser572delinsMet
ENST00000315422.9:c.1710_1715del ENSP00000323747.4:p.Ile570_Ser572delinsMet
ENST00000377313.6:c.1725_1730del ENSP00000366530.1:p.Ile575_Ser577delinsMet
ENST00000440873.6:c.1710_1715del ENSP00000413944.2:p.Ile570_Ser572delinsMet
ENST00000450708.7:c.1710_1715del MANE Select ENSP00000394933.3:p.Ile570_Ser572delinsMet
ENST00000478548.2:n.2211_2216del
ENST00000671939.1:n.1987_1992del
ENST00000672304.1:c.1836_1841del ENSP00000500585.1:p.Ile612_Ser614delinsMet
ENST00000312049.10:c.1710_1715del ENSP00000308975.6:p.Ile570_Ser572delinsMet
ENST00000315422.8:c.1710_1715del ENSP00000323747.4:p.Ile570_Ser572delinsMet
ENST00000337652.5:c.1725_1730del ENSP00000337088.1:p.Ile575_Ser577delinsMet
ENST00000377313.5:c.1725_1730del ENSP00000366530.1:p.Ile575_Ser577delinsMet
ENST00000377316.6:c.1545_1550del ENSP00000366533.1:p.Ile515_Ser517delinsMet
ENST00000377321.5:c.1605_1610del ENSP00000366538.1:p.Ile535_Ser537delinsMet
ENST00000377326.7:c.1710_1715del ENSP00000366543.3:p.Ile570_Ser572delinsMet
ENST00000394374.6:c.1725_1730del ENSP00000377899.2:p.Ile575_Ser577delinsMet
ENST00000394376.5:c.1725_1730del ENSP00000377901.1:p.Ile575_Ser577delinsMet
ENST00000478548.1:n.1259_1264del
NM_000244.3:c.1725_1730del , LRG_509t1:c.1725_1730del NP_000235.2:p.Ile575_Ser577delinsMet
NM_130799.2:c.1710_1715del , LRG_509t2:c.1710_1715del NP_570711.1:p.Ile570_Ser572delinsMet
NM_130800.2:c.1725_1730del NP_570712.1:p.Ile575_Ser577delinsMet
NM_130801.2:c.1725_1730del NP_570713.1:p.Ile575_Ser577delinsMet
NM_130802.2:c.1725_1730del NP_570714.1:p.Ile575_Ser577delinsMet
NM_130803.2:c.1725_1730del NP_570715.1:p.Ile575_Ser577delinsMet
NM_130804.2:c.1725_1730del NP_570716.1:p.Ile575_Ser577delinsMet
XM_005274001.3:c.1710_1715del XP_005274058.1:p.Ile570_Ser572delinsMet
XM_011545040.1:c.1836_1841del XP_011543342.1:p.Ile612_Ser614delinsMet
XM_011545041.1:c.1836_1841del XP_011543343.1:p.Ile612_Ser614delinsMet
XM_011545042.1:c.1836_1841del XP_011543344.1:p.Ile612_Ser614delinsMet
XM_005274001.4:c.1710_1715del XP_005274058.1:p.Ile570_Ser572delinsMet
XM_011545041.2:c.1836_1841del XP_011543343.1:p.Ile612_Ser614delinsMet
XM_011545042.3:c.1836_1841del XP_011543344.1:p.Ile612_Ser614delinsMet
XM_017017765.1:c.1851_1856del XP_016873254.1:p.Ile617_Ser619delinsMet
XM_017017766.1:c.1851_1856del XP_016873255.1:p.Ile617_Ser619delinsMet
XM_017017767.2:c.1851_1856del XP_016873256.1:p.Ile617_Ser619delinsMet
XM_017017768.1:c.1851_1856del XP_016873257.1:p.Ile617_Ser619delinsMet
XM_017017769.1:c.1710_1715del XP_016873258.1:p.Ile570_Ser572delinsMet
XM_017017770.2:c.1710_1715del XP_016873259.1:p.Ile570_Ser572delinsMet
NM_001370251.1:c.1836_1841del NP_001357180.1:p.Ile612_Ser614delinsMet
NM_001370259.2:c.1710_1715del MANE Select NP_001357188.2:p.Ile570_Ser572delinsMet
NM_001370260.1:c.1710_1715del NP_001357189.1:p.Ile570_Ser572delinsMet
NM_001370261.1:c.1710_1715del NP_001357190.1:p.Ile570_Ser572delinsMet
NM_001370262.1:c.1605_1610del NP_001357191.1:p.Ile535_Ser537delinsMet
NM_001370263.1:c.1605_1610del NP_001357192.1:p.Ile535_Ser537delinsMet
NM_000244.4:c.1725_1730del NP_000235.3:p.Ile575_Ser577delinsMet
NM_001370251.2:c.1836_1841del NP_001357180.2:p.Ile612_Ser614delinsMet
NM_001370260.2:c.1710_1715del NP_001357189.2:p.Ile570_Ser572delinsMet
NM_001370261.2:c.1710_1715del NP_001357190.2:p.Ile570_Ser572delinsMet
NM_001370262.2:c.1605_1610del NP_001357191.2:p.Ile535_Ser537delinsMet
NM_001370263.2:c.1605_1610del NP_001357192.2:p.Ile535_Ser537delinsMet
NM_130799.3:c.1710_1715del NP_570711.2:p.Ile570_Ser572delinsMet
NM_130800.3:c.1725_1730del NP_570712.2:p.Ile575_Ser577delinsMet
NM_130801.3:c.1725_1730del NP_570713.2:p.Ile575_Ser577delinsMet
NM_130802.3:c.1725_1730del NP_570714.2:p.Ile575_Ser577delinsMet
NM_130803.3:c.1725_1730del NP_570715.2:p.Ile575_Ser577delinsMet
NM_130804.3:c.1725_1730del NP_570716.2:p.Ile575_Ser577delinsMet