Canonical Allele Identifier: CA343805985

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634807A>T (hg19) ; chr1:g.172665667A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665667A>T , CM000663.2:g.172665667A>T	GRCh38
NC_000001.10:g.172634807A>T , CM000663.1:g.172634807A>T	GRCh37
NC_000001.9:g.170901430A>T	NCBI36
NG_007269.1:g.11623A>T , LRG_58:g.11623A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.497A>T MANE Select	ENSP00000356694.2:p.Tyr166Phe
ENST00000340030.4:c.*67A>T	ENSP00000344739.3:n.*67A>T
ENST00000367721.2:c.497A>T	ENSP00000356694.2:p.Tyr166Phe
NM_000639.2:c.497A>T	NP_000630.1:p.Tyr166Phe
NM_001302746.1:c.*67A>T	NP_001289675.1:n.*67A>T
NM_000639.3:c.497A>T MANE Select	NP_000630.1:p.Tyr166Phe
NM_001302746.2:c.*67A>T	NP_001289675.1:n.*67A>T