Canonical Allele Identifier: CA343806172

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634894T>G (hg19) ; chr1:g.172665754T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665754T>G , CM000663.2:g.172665754T>G	GRCh38
NC_000001.10:g.172634894T>G , CM000663.1:g.172634894T>G	GRCh37
NC_000001.9:g.170901517T>G	NCBI36
NG_007269.1:g.11710T>G , LRG_58:g.11710T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.584T>G MANE Select	ENSP00000356694.2:p.Val195Gly
ENST00000340030.4:c.*154T>G	ENSP00000344739.3:n.*154T>G
ENST00000367721.2:c.584T>G	ENSP00000356694.2:p.Val195Gly
NM_000639.2:c.584T>G	NP_000630.1:p.Val195Gly
NM_001302746.1:c.*154T>G	NP_001289675.1:n.*154T>G
NM_000639.3:c.584T>G MANE Select	NP_000630.1:p.Val195Gly
NM_001302746.2:c.*154T>G	NP_001289675.1:n.*154T>G