Canonical Allele Identifier: CA32979649
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs55728520

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665819A>G , CM000663.2:g.172665819A>G GRCh38
NC_000001.10:g.172634959A>G , CM000663.1:g.172634959A>G GRCh37
NC_000001.9:g.170901582A>G NCBI36
NG_007269.1:g.11775A>G , LRG_58:g.11775A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.649A>G MANE Select ENSP00000356694.2:p.Lys217Glu
ENST00000340030.4:c.*219A>G ENSP00000344739.3:n.*219A>G
ENST00000367721.2:c.649A>G ENSP00000356694.2:p.Lys217Glu
NM_000639.2:c.649A>G NP_000630.1:p.Lys217Glu
NM_001302746.1:c.*219A>G NP_001289675.1:n.*219A>G
NM_000639.3:c.649A>G MANE Select NP_000630.1:p.Lys217Glu
NM_001302746.2:c.*219A>G NP_001289675.1:n.*219A>G