Canonical Allele Identifier: CA421944467

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634871G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665731G>T , CM000663.2:g.172665731G>T	GRCh38
NC_000001.10:g.172634871G>T , CM000663.1:g.172634871G>T	GRCh37
NC_000001.9:g.170901494G>T	NCBI36
NG_007269.1:g.11687G>T , LRG_58:g.11687G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.561G>T MANE Select	ENSP00000356694.2:p.Gly187=
ENST00000340030.4:c.*131G>T	ENSP00000344739.3:n.*131G>T
ENST00000367721.2:c.561G>T	ENSP00000356694.2:p.Gly187=
NM_000639.2:c.561G>T	NP_000630.1:p.Gly187=
NM_001302746.1:c.*131G>T	NP_001289675.1:n.*131G>T
NM_000639.3:c.561G>T MANE Select	NP_000630.1:p.Gly187=
NM_001302746.2:c.*131G>T	NP_001289675.1:n.*131G>T