Canonical Allele Identifier: CA343805961
Gene: FASLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665657G>A , CM000663.2:g.172665657G>A GRCh38
NC_000001.10:g.172634797G>A , CM000663.1:g.172634797G>A GRCh37
NC_000001.9:g.170901420G>A NCBI36
NG_007269.1:g.11613G>A , LRG_58:g.11613G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.487G>A MANE Select ENSP00000356694.2:p.Glu163Lys
ENST00000340030.4:c.*57G>A ENSP00000344739.3:n.*57G>A
ENST00000367721.2:c.487G>A ENSP00000356694.2:p.Glu163Lys
NM_000639.2:c.487G>A NP_000630.1:p.Glu163Lys
NM_001302746.1:c.*57G>A NP_001289675.1:n.*57G>A
NM_000639.3:c.487G>A MANE Select NP_000630.1:p.Glu163Lys
NM_001302746.2:c.*57G>A NP_001289675.1:n.*57G>A