Canonical Allele Identifier: CA343806085
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs1252955103

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665714G>A , CM000663.2:g.172665714G>A GRCh38
NC_000001.10:g.172634854G>A , CM000663.1:g.172634854G>A GRCh37
NC_000001.9:g.170901477G>A NCBI36
NG_007269.1:g.11670G>A , LRG_58:g.11670G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.544G>A MANE Select ENSP00000356694.2:p.Val182Met
ENST00000340030.4:c.*114G>A ENSP00000344739.3:n.*114G>A
ENST00000367721.2:c.544G>A ENSP00000356694.2:p.Val182Met
NM_000639.2:c.544G>A NP_000630.1:p.Val182Met
NM_001302746.1:c.*114G>A NP_001289675.1:n.*114G>A
NM_000639.3:c.544G>A MANE Select NP_000630.1:p.Val182Met
NM_001302746.2:c.*114G>A NP_001289675.1:n.*114G>A