Canonical Allele Identifier: CA343805980

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634804C>G (hg19) ; chr1:g.172665664C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665664C>G , CM000663.2:g.172665664C>G	GRCh38
NC_000001.10:g.172634804C>G , CM000663.1:g.172634804C>G	GRCh37
NC_000001.9:g.170901427C>G	NCBI36
NG_007269.1:g.11620C>G , LRG_58:g.11620C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.494C>G MANE Select	ENSP00000356694.2:p.Thr165Ser
ENST00000340030.4:c.*64C>G	ENSP00000344739.3:n.*64C>G
ENST00000367721.2:c.494C>G	ENSP00000356694.2:p.Thr165Ser
NM_000639.2:c.494C>G	NP_000630.1:p.Thr165Ser
NM_001302746.1:c.*64C>G	NP_001289675.1:n.*64C>G
NM_000639.3:c.494C>G MANE Select	NP_000630.1:p.Thr165Ser
NM_001302746.2:c.*64C>G	NP_001289675.1:n.*64C>G