Canonical Allele Identifier: CA2695214556
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735647
ClinVar RCV Id: RCV003518776

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64804815_64804820del , CM000673.2:g.64804815_64804820del GRCh38
NC_000011.9:g.64572287_64572292del , CM000673.1:g.64572287_64572292del GRCh37
NC_000011.8:g.64328863_64328868del NCBI36
NG_008929.1:g.11475_11480del , LRG_509:g.11475_11480del
NG_033040.1:g.3422_3427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000377313.7:c.1366-4_1367del
ENST00000394374.8:c.*659-4_*660del
ENST00000394376.7:c.1351-13_1351-8del ENSP00000377901.3:n.1351-13_1351-8del
ENST00000413626.2:c.1351-4_1352del
ENST00000424912.2:c.1351-4_1352del
ENST00000429702.6:c.1351-4_1352del
ENST00000672079.2:c.*447-4_*448del
ENST00000710881.1:c.1366-4_1367del
ENST00000394374.7:c.1098-4_1099del
ENST00000394376.6:c.702-13_702-8del
ENST00000478548.3:n.1844-4_1845del
ENST00000671939.2:n.1313-4_1314del
ENST00000671965.2:n.1733-4_1734del
ENST00000312049.11:c.1351-4_1352del
ENST00000315422.9:c.1351-4_1352del
ENST00000377313.6:c.1366-4_1367del
ENST00000440873.6:c.1351-4_1352del
ENST00000450708.7:c.1351-4_1352del
ENST00000478548.2:n.1852-4_1853del
ENST00000671939.1:n.1628-4_1629del
ENST00000672079.1:c.1226-4_1227del
ENST00000672304.1:c.1477-4_1478del
ENST00000312049.10:c.1351-4_1352del
ENST00000315422.8:c.1351-4_1352del
ENST00000337652.5:c.1366-4_1367del
ENST00000377313.5:c.1366-4_1367del
ENST00000377316.6:c.1186-4_1187del
ENST00000377321.5:c.1246-4_1247del
ENST00000377326.7:c.1351-4_1352del
ENST00000394374.6:c.1366-4_1367del
ENST00000394376.5:c.1366-4_1367del
ENST00000478548.1:n.900-4_901del
NM_000244.3:c.1366-4_1367del , LRG_509t1:c.1366-4_1367del
NM_130799.2:c.1351-4_1352del , LRG_509t2:c.1351-4_1352del
NM_130800.2:c.1366-4_1367del
NM_130801.2:c.1366-4_1367del
NM_130802.2:c.1366-4_1367del
NM_130803.2:c.1366-4_1367del
NM_130804.2:c.1366-4_1367del
XM_005274001.3:c.1351-4_1352del
XM_011545040.1:c.1477-4_1478del
XM_011545041.1:c.1477-4_1478del
XM_011545042.1:c.1477-4_1478del
XM_005274001.4:c.1351-4_1352del
XM_011545041.2:c.1477-4_1478del
XM_011545042.3:c.1477-4_1478del
XM_017017765.1:c.1492-4_1493del
XM_017017766.1:c.1492-4_1493del
XM_017017767.2:c.1492-4_1493del
XM_017017768.1:c.1492-4_1493del
XM_017017769.1:c.1351-4_1352del
XM_017017770.2:c.1351-4_1352del
NM_001370251.1:c.1477-4_1478del
NM_001370259.2:c.1351-4_1352del
NM_001370260.1:c.1351-4_1352del
NM_001370261.1:c.1351-4_1352del
NM_001370262.1:c.1246-4_1247del
NM_001370263.1:c.1246-4_1247del
NM_000244.4:c.1366-4_1367del
NM_001370251.2:c.1477-4_1478del
NM_001370260.2:c.1351-4_1352del
NM_001370261.2:c.1351-4_1352del
NM_001370262.2:c.1246-4_1247del
NM_001370263.2:c.1246-4_1247del
NM_130799.3:c.1351-4_1352del
NM_130800.3:c.1366-4_1367del
NM_130801.3:c.1366-4_1367del
NM_130802.3:c.1366-4_1367del
NM_130803.3:c.1366-4_1367del
NM_130804.3:c.1366-4_1367del