Canonical Allele Identifier: CA343805973
Gene: FASLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665661A>T , CM000663.2:g.172665661A>T GRCh38
NC_000001.10:g.172634801A>T , CM000663.1:g.172634801A>T GRCh37
NC_000001.9:g.170901424A>T NCBI36
NG_007269.1:g.11617A>T , LRG_58:g.11617A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.491A>T MANE Select ENSP00000356694.2:p.Asp164Val
ENST00000340030.4:c.*61A>T ENSP00000344739.3:n.*61A>T
ENST00000367721.2:c.491A>T ENSP00000356694.2:p.Asp164Val
NM_000639.2:c.491A>T NP_000630.1:p.Asp164Val
NM_001302746.1:c.*61A>T NP_001289675.1:n.*61A>T
NM_000639.3:c.491A>T MANE Select NP_000630.1:p.Asp164Val
NM_001302746.2:c.*61A>T NP_001289675.1:n.*61A>T