Canonical Allele Identifier: CA1207431698

Gene: FASLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665816T= , CM000663.2:g.172665816T=	GRCh38
NC_000001.10:g.172634956T= , CM000663.1:g.172634956T=	GRCh37
NC_000001.9:g.170901579T=	NCBI36
NG_007269.1:g.11772T= , LRG_58:g.11772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.646T= MANE Select	ENSP00000356694.2:p.Ser216=
ENST00000340030.4:c.*216T=	ENSP00000344739.3:n.*216T=
ENST00000367721.2:c.646T=	ENSP00000356694.2:p.Ser216=
NM_000639.2:c.646T=	NP_000630.1:p.Ser216=
NM_001302746.1:c.*216T=	NP_001289675.1:n.*216T=
NM_000639.3:c.646T= MANE Select	NP_000630.1:p.Ser216=
NM_001302746.2:c.*216T=	NP_001289675.1:n.*216T=