Canonical Allele Identifier: CA017625
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 201001
dbSNP Id: rs764570645

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64805033_64805043del , CM000673.2:g.64805033_64805043del GRCh38
NC_000011.9:g.64572505_64572515del , CM000673.1:g.64572505_64572515del GRCh37
NC_000011.8:g.64329081_64329091del NCBI36
NG_008929.1:g.11262_11272del , LRG_509:g.11262_11272del
NG_033040.1:g.3209_3219del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377313.7:c.1365+1_1365+11del
ENST00000394374.8:c.*658+1_*658+11del
ENST00000394376.7:c.1350+1_1350+11del
ENST00000413626.2:c.1350+1_1350+11del
ENST00000424912.2:c.1350+1_1350+11del
ENST00000429702.6:c.1350+1_1350+11del
ENST00000672079.2:c.*446+1_*446+11del
ENST00000710881.1:c.1365+1_1365+11del
ENST00000394374.7:c.1097+1_1097+11del
ENST00000394376.6:c.701+1_701+11del
ENST00000478548.3:n.1843+1_1843+11del
ENST00000671939.2:n.1312+1_1312+11del
ENST00000671965.2:n.1732+1_1732+11del
ENST00000312049.11:c.1350+1_1350+11del
ENST00000315422.9:c.1350+1_1350+11del
ENST00000377313.6:c.1365+1_1365+11del
ENST00000440873.6:c.1350+1_1350+11del
ENST00000450708.7:c.1350+1_1350+11del
ENST00000478548.2:n.1851+1_1851+11del
ENST00000671939.1:n.1627+1_1627+11del
ENST00000672079.1:c.1225+1_1225+11del
ENST00000672304.1:c.1476+1_1476+11del
ENST00000312049.10:c.1350+1_1350+11del
ENST00000315422.8:c.1350+1_1350+11del
ENST00000337652.5:c.1365+1_1365+11del
ENST00000377313.5:c.1365+1_1365+11del
ENST00000377316.6:c.1186-217_1186-207del ENSP00000366533.1:n.1186-217_1186-207del
ENST00000377321.5:c.1245+1_1245+11del
ENST00000377326.7:c.1350+1_1350+11del
ENST00000394374.6:c.1365+1_1365+11del
ENST00000394376.5:c.1365+1_1365+11del
ENST00000478548.1:n.899+1_899+11del
NM_000244.3:c.1365+1_1365+11del , LRG_509t1:c.1365+1_1365+11del
NM_130799.2:c.1350+1_1350+11del , LRG_509t2:c.1350+1_1350+11del
NM_130800.2:c.1365+1_1365+11del
NM_130801.2:c.1365+1_1365+11del
NM_130802.2:c.1365+1_1365+11del
NM_130803.2:c.1365+1_1365+11del
NM_130804.2:c.1365+1_1365+11del
XM_005274001.3:c.1350+1_1350+11del
XM_011545040.1:c.1476+1_1476+11del
XM_011545041.1:c.1476+1_1476+11del
XM_011545042.1:c.1476+1_1476+11del
XM_005274001.4:c.1350+1_1350+11del
XM_011545041.2:c.1476+1_1476+11del
XM_011545042.3:c.1476+1_1476+11del
XM_017017765.1:c.1491+1_1491+11del
XM_017017766.1:c.1491+1_1491+11del
XM_017017767.2:c.1491+1_1491+11del
XM_017017768.1:c.1491+1_1491+11del
XM_017017769.1:c.1350+1_1350+11del
XM_017017770.2:c.1350+1_1350+11del
NM_001370251.1:c.1476+1_1476+11del
NM_001370259.2:c.1350+1_1350+11del
NM_001370260.1:c.1350+1_1350+11del
NM_001370261.1:c.1350+1_1350+11del
NM_001370262.1:c.1245+1_1245+11del
NM_001370263.1:c.1245+1_1245+11del
NM_000244.4:c.1365+1_1365+11del
NM_001370251.2:c.1476+1_1476+11del
NM_001370260.2:c.1350+1_1350+11del
NM_001370261.2:c.1350+1_1350+11del
NM_001370262.2:c.1245+1_1245+11del
NM_001370263.2:c.1245+1_1245+11del
NM_130799.3:c.1350+1_1350+11del
NM_130800.3:c.1365+1_1365+11del
NM_130801.3:c.1365+1_1365+11del
NM_130802.3:c.1365+1_1365+11del
NM_130803.3:c.1365+1_1365+11del
NM_130804.3:c.1365+1_1365+11del