Canonical Allele Identifier: CA658656152
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 457345
ClinVar RCV Id: RCV000556751

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64805997_64806341del , CM000673.2:g.64805997_64806341del GRCh38
NC_000011.9:g.64573469_64573813del , CM000673.1:g.64573469_64573813del GRCh37
NC_000011.8:g.64330045_64330389del NCBI36
NG_008929.1:g.9954_10298del , LRG_509:g.9954_10298del
NG_033040.1:g.1901_2245del

Transcript Alleles

HGVS Amino-acid change
ENST00000377313.7:c.955_1065-227del
ENST00000394374.8:c.*248_*358-227del
ENST00000394376.7:c.940_1050-227del
ENST00000413626.2:c.940_1050-227del
ENST00000424912.2:c.940_1050-227del
ENST00000429702.6:c.940_1050-227del
ENST00000672079.2:c.940_*145+86del
ENST00000710881.1:c.955_1065-227del
ENST00000394374.7:c.687_797-227del
ENST00000394376.6:c.291_401-227del
ENST00000478548.3:n.972_1316del
ENST00000671939.2:n.902_1012-227del
ENST00000671965.2:n.1322_1432-227del
ENST00000312049.11:c.940_1050-227del
ENST00000315422.9:c.940_1050-227del
ENST00000377313.6:c.955_1065-227del
ENST00000440873.6:c.940_1050-227del
ENST00000450708.7:c.940_1050-227del
ENST00000478548.2:n.980_1324del
ENST00000671939.1:n.1217_1327-227del
ENST00000672079.1:c.666_924+86del
ENST00000672304.1:c.940_1066del
ENST00000312049.10:c.940_1050-227del
ENST00000315422.8:c.940_1050-227del
ENST00000337652.5:c.955_1065-227del
ENST00000377313.5:c.955_1065-227del
ENST00000377316.6:c.940_1050-227del
ENST00000377321.5:c.835_945-227del
ENST00000377326.7:c.940_1050-227del
ENST00000394374.6:c.955_1065-227del
ENST00000394376.5:c.955_1065-227del
ENST00000478548.1:n.28_372del
NM_000244.3:c.955_1065-227del , LRG_509t1:c.955_1065-227del
NM_130799.2:c.940_1050-227del , LRG_509t2:c.940_1050-227del
NM_130800.2:c.955_1065-227del
NM_130801.2:c.955_1065-227del
NM_130802.2:c.955_1065-227del
NM_130803.2:c.955_1065-227del
NM_130804.2:c.955_1065-227del
XM_005274001.3:c.940_1050-227del
XM_011545040.1:c.940_1066del
XM_011545041.1:c.940_1066del
XM_011545042.1:c.940_1066del
XM_005274001.4:c.940_1050-227del
XM_011545041.2:c.940_1066del
XM_011545042.3:c.940_1066del
XM_017017765.1:c.955_1081del
XM_017017766.1:c.955_1081del
XM_017017767.2:c.955_1081del
XM_017017768.1:c.955_1081del
XM_017017769.1:c.940_1050-227del
XM_017017770.2:c.940_1050-227del
NM_001370251.1:c.940_1066del
NM_001370259.2:c.940_1050-227del
NM_001370260.1:c.940_1050-227del
NM_001370261.1:c.940_1050-227del
NM_001370262.1:c.835_945-227del
NM_001370263.1:c.835_945-227del
NM_000244.4:c.955_1065-227del
NM_001370251.2:c.940_1066del
NM_001370260.2:c.940_1050-227del
NM_001370261.2:c.940_1050-227del
NM_001370262.2:c.835_945-227del
NM_001370263.2:c.835_945-227del
NM_130799.3:c.940_1050-227del
NM_130800.3:c.955_1065-227del
NM_130801.3:c.955_1065-227del
NM_130802.3:c.955_1065-227del
NM_130803.3:c.955_1065-227del
NM_130804.3:c.955_1065-227del