Canonical Allele Identifier: CA421944442

Gene: FASLG

Linked Data

• dbSNP Id: rs1659243370
• MyVariant Identifiers: chr1:g.172634829A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665689A>G , CM000663.2:g.172665689A>G	GRCh38
NC_000001.10:g.172634829A>G , CM000663.1:g.172634829A>G	GRCh37
NC_000001.9:g.170901452A>G	NCBI36
NG_007269.1:g.11645A>G , LRG_58:g.11645A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.519A>G MANE Select	ENSP00000356694.2:p.Gly173=
ENST00000340030.4:c.*89A>G	ENSP00000344739.3:n.*89A>G
ENST00000367721.2:c.519A>G	ENSP00000356694.2:p.Gly173=
NM_000639.2:c.519A>G	NP_000630.1:p.Gly173=
NM_001302746.1:c.*89A>G	NP_001289675.1:n.*89A>G
NM_000639.3:c.519A>G MANE Select	NP_000630.1:p.Gly173=
NM_001302746.2:c.*89A>G	NP_001289675.1:n.*89A>G