Canonical Allele Identifier: CA1207431647
Gene: FASLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665652A= , CM000663.2:g.172665652A= GRCh38
NC_000001.10:g.172634792A= , CM000663.1:g.172634792A= GRCh37
NC_000001.9:g.170901415A= NCBI36
NG_007269.1:g.11608A= , LRG_58:g.11608A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.482A= MANE Select ENSP00000356694.2:p.Glu161=
ENST00000340030.4:c.*52A= ENSP00000344739.3:n.*52A=
ENST00000367721.2:c.482A= ENSP00000356694.2:p.Glu161=
NM_000639.2:c.482A= NP_000630.1:p.Glu161=
NM_001302746.1:c.*52A= NP_001289675.1:n.*52A=
NM_000639.3:c.482A= MANE Select NP_000630.1:p.Glu161=
NM_001302746.2:c.*52A= NP_001289675.1:n.*52A=