Canonical Allele Identifier: CA16043460
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374107
ClinVar RCV Id: RCV000415413
dbSNP Id: rs1057518903

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64807892del , CM000673.2:g.64807892del GRCh38
NC_000011.9:g.64575364del , CM000673.1:g.64575364del GRCh37
NC_000011.8:g.64331940del NCBI36
NG_008929.1:g.8405del , LRG_509:g.8405del
NG_033040.1:g.352del

Transcript Alleles

HGVS Amino-acid change
ENST00000312049.11:c.654+1del
ENST00000315422.9:c.654+1del
ENST00000377313.6:c.669+1del
ENST00000440873.6:c.654+1del
ENST00000450708.7:c.654+1del
ENST00000478548.2:n.694+1del
ENST00000671939.1:n.722del
ENST00000671965.1:n.314+1del
ENST00000672079.1:n.380+1del
ENST00000672304.1:c.654+1del
ENST00000312049.10:c.654+1del
ENST00000315422.8:c.654+1del
ENST00000337652.5:c.669+1del
ENST00000377313.5:c.669+1del
ENST00000377316.6:c.654+1del
ENST00000377321.5:c.549+106del ENSP00000366538.1:p.=
ENST00000377326.7:c.654+1del
ENST00000394374.6:c.669+1del
ENST00000394376.5:c.669+1del
ENST00000413626.1:c.654+1del
ENST00000440873.5:c.654+1del
ENST00000450708.5:c.654+1del
NM_000244.3:c.669+1del , LRG_509t1:c.669+1del
NM_130799.2:c.654+1del , LRG_509t2:c.654+1del
NM_130800.2:c.669+1del
NM_130801.2:c.669+1del
NM_130802.2:c.669+1del
NM_130803.2:c.669+1del
NM_130804.2:c.669+1del
XM_005274001.3:c.654+1del
XM_011545040.1:c.654+1del
XM_011545041.1:c.654+1del
XM_011545042.1:c.654+1del
XM_005274001.4:c.654+1del
XM_011545041.2:c.654+1del
XM_011545042.3:c.654+1del
XM_017017765.1:c.669+1del
XM_017017766.1:c.669+1del
XM_017017767.2:c.669+1del
XM_017017768.1:c.669+1del
XM_017017769.1:c.654+1del
XM_017017770.2:c.654+1del
NM_001370251.1:c.654+1del
NM_001370259.2:c.654+1del
NM_001370260.1:c.654+1del
NM_001370261.1:c.654+1del
NM_001370262.1:c.549+106del NP_001357191.1:p.=
NM_001370263.1:c.549+106del NP_001357192.1:p.=