Canonical Allele Identifier: CA2499221144

Gene: MEN1

Linked Data

• ClinVar Variation Id: 1066873
• ClinVar RCV Id: RCV001377991 ; RCV001810728
• dbSNP Id: rs2136094253

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64804808_64804819del , CM000673.2:g.64804808_64804819del	GRCh38
NC_000011.9:g.64572280_64572291del , CM000673.1:g.64572280_64572291del	GRCh37
NC_000011.8:g.64328856_64328867del	NCBI36
NG_008929.1:g.11476_11487del , LRG_509:g.11476_11487del
NG_033040.1:g.3423_3434del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377313.7:c.1366-3_1374del
ENST00000394374.8:c.*659-3_*667del
ENST00000394376.7:c.1351-12_1351-1del	ENSP00000377901.3:n.1351-12_1351-1del
ENST00000413626.2:c.1351-3_1359del
ENST00000424912.2:c.1351-3_1359del
ENST00000429702.6:c.1351-3_1359del
ENST00000672079.2:c.*447-3_*455del
ENST00000710881.1:c.1366-3_1374del
ENST00000394374.7:c.1098-3_1106del
ENST00000394376.6:c.702-12_702-1del
ENST00000478548.3:n.1844-3_1852del
ENST00000671939.2:n.1313-3_1321del
ENST00000671965.2:n.1733-3_1741del
ENST00000312049.11:c.1351-3_1359del
ENST00000315422.9:c.1351-3_1359del
ENST00000377313.6:c.1366-3_1374del
ENST00000440873.6:c.1351-3_1359del
ENST00000450708.7:c.1351-3_1359del
ENST00000478548.2:n.1852-3_1860del
ENST00000671939.1:n.1628-3_1636del
ENST00000672079.1:c.1226-3_1234del
ENST00000672304.1:c.1477-3_1485del
ENST00000312049.10:c.1351-3_1359del
ENST00000315422.8:c.1351-3_1359del
ENST00000337652.5:c.1366-3_1374del
ENST00000377313.5:c.1366-3_1374del
ENST00000377316.6:c.1186-3_1194del
ENST00000377321.5:c.1246-3_1254del
ENST00000377326.7:c.1351-3_1359del
ENST00000394374.6:c.1366-3_1374del
ENST00000394376.5:c.1366-3_1374del
ENST00000478548.1:n.900-3_908del
NM_000244.3:c.1366-3_1374del , LRG_509t1:c.1366-3_1374del
NM_130799.2:c.1351-3_1359del , LRG_509t2:c.1351-3_1359del
NM_130800.2:c.1366-3_1374del
NM_130801.2:c.1366-3_1374del
NM_130802.2:c.1366-3_1374del
NM_130803.2:c.1366-3_1374del
NM_130804.2:c.1366-3_1374del
XM_005274001.3:c.1351-3_1359del
XM_011545040.1:c.1477-3_1485del
XM_011545041.1:c.1477-3_1485del
XM_011545042.1:c.1477-3_1485del
XM_005274001.4:c.1351-3_1359del
XM_011545041.2:c.1477-3_1485del
XM_011545042.3:c.1477-3_1485del
XM_017017765.1:c.1492-3_1500del
XM_017017766.1:c.1492-3_1500del
XM_017017767.2:c.1492-3_1500del
XM_017017768.1:c.1492-3_1500del
XM_017017769.1:c.1351-3_1359del
XM_017017770.2:c.1351-3_1359del
NM_001370251.1:c.1477-3_1485del
NM_001370259.2:c.1351-3_1359del
NM_001370260.1:c.1351-3_1359del
NM_001370261.1:c.1351-3_1359del
NM_001370262.1:c.1246-3_1254del
NM_001370263.1:c.1246-3_1254del
NM_000244.4:c.1366-3_1374del
NM_001370251.2:c.1477-3_1485del
NM_001370260.2:c.1351-3_1359del
NM_001370261.2:c.1351-3_1359del
NM_001370262.2:c.1246-3_1254del
NM_001370263.2:c.1246-3_1254del
NM_130799.3:c.1351-3_1359del
NM_130800.3:c.1366-3_1374del
NM_130801.3:c.1366-3_1374del
NM_130802.3:c.1366-3_1374del
NM_130803.3:c.1366-3_1374del
NM_130804.3:c.1366-3_1374del