Canonical Allele Identifier: CA1207431653

Gene: FASLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665668T= , CM000663.2:g.172665668T=	GRCh38
NC_000001.10:g.172634808T= , CM000663.1:g.172634808T=	GRCh37
NC_000001.9:g.170901431T=	NCBI36
NG_007269.1:g.11624T= , LRG_58:g.11624T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.498T= MANE Select	ENSP00000356694.2:p.Tyr166=
ENST00000340030.4:c.*68T=	ENSP00000344739.3:n.*68T=
ENST00000367721.2:c.498T=	ENSP00000356694.2:p.Tyr166=
NM_000639.2:c.498T=	NP_000630.1:p.Tyr166=
NM_001302746.1:c.*68T=	NP_001289675.1:n.*68T=
NM_000639.3:c.498T= MANE Select	NP_000630.1:p.Tyr166=
NM_001302746.2:c.*68T=	NP_001289675.1:n.*68T=