Canonical Allele Identifier: CA343806234

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634921A>T (hg19) ; chr1:g.172665781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665781A>T , CM000663.2:g.172665781A>T	GRCh38
NC_000001.10:g.172634921A>T , CM000663.1:g.172634921A>T	GRCh37
NC_000001.9:g.170901544A>T	NCBI36
NG_007269.1:g.11737A>T , LRG_58:g.11737A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.611A>T MANE Select	ENSP00000356694.2:p.Asn204Ile
ENST00000340030.4:c.*181A>T	ENSP00000344739.3:n.*181A>T
ENST00000367721.2:c.611A>T	ENSP00000356694.2:p.Asn204Ile
NM_000639.2:c.611A>T	NP_000630.1:p.Asn204Ile
NM_001302746.1:c.*181A>T	NP_001289675.1:n.*181A>T
NM_000639.3:c.611A>T MANE Select	NP_000630.1:p.Asn204Ile
NM_001302746.2:c.*181A>T	NP_001289675.1:n.*181A>T