Canonical Allele Identifier: CA2649137841

Gene: FASLG

Linked Data

• gnomAD v4: 1-172664215-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172664215A>G , CM000663.2:g.172664215A>G	GRCh38
NC_000001.10:g.172633355A>G , CM000663.1:g.172633355A>G	GRCh37
NC_000001.9:g.170899978A>G	NCBI36
NG_007269.1:g.10171A>G , LRG_58:g.10171A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.395-119A>G MANE Select	ENSP00000356694.2:n.395-119A>G
ENST00000340030.4:c.349-119A>G	ENSP00000344739.3:n.349-119A>G
ENST00000367721.2:c.395-119A>G	ENSP00000356694.2:n.395-119A>G
NM_000639.2:c.395-119A>G	NP_000630.1:n.395-119A>G
NM_001302746.1:c.349-119A>G	NP_001289675.1:n.349-119A>G
NM_000639.3:c.395-119A>G MANE Select	NP_000630.1:n.395-119A>G
NM_001302746.2:c.349-119A>G	NP_001289675.1:n.349-119A>G