Canonical Allele Identifier: CA343806165

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634892A>T (hg19) ; chr1:g.172665752A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665752A>T , CM000663.2:g.172665752A>T	GRCh38
NC_000001.10:g.172634892A>T , CM000663.1:g.172634892A>T	GRCh37
NC_000001.9:g.170901515A>T	NCBI36
NG_007269.1:g.11708A>T , LRG_58:g.11708A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.582A>T MANE Select	ENSP00000356694.2:p.Lys194Asn
ENST00000340030.4:c.*152A>T	ENSP00000344739.3:n.*152A>T
ENST00000367721.2:c.582A>T	ENSP00000356694.2:p.Lys194Asn
NM_000639.2:c.582A>T	NP_000630.1:p.Lys194Asn
NM_001302746.1:c.*152A>T	NP_001289675.1:n.*152A>T
NM_000639.3:c.582A>T MANE Select	NP_000630.1:p.Lys194Asn
NM_001302746.2:c.*152A>T	NP_001289675.1:n.*152A>T