Canonical Allele Identifier: CA421944398

Gene: FASLG

Linked Data

• MyVariant Identifiers: chr1:g.172634769C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665629C>T , CM000663.2:g.172665629C>T	GRCh38
NC_000001.10:g.172634769C>T , CM000663.1:g.172634769C>T	GRCh37
NC_000001.9:g.170901392C>T	NCBI36
NG_007269.1:g.11585C>T , LRG_58:g.11585C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.459C>T MANE Select	ENSP00000356694.2:p.Ser153=
ENST00000340030.4:c.*29C>T	ENSP00000344739.3:n.*29C>T
ENST00000367721.2:c.459C>T	ENSP00000356694.2:p.Ser153=
NM_000639.2:c.459C>T	NP_000630.1:p.Ser153=
NM_001302746.1:c.*29C>T	NP_001289675.1:n.*29C>T
NM_000639.3:c.459C>T MANE Select	NP_000630.1:p.Ser153=
NM_001302746.2:c.*29C>T	NP_001289675.1:n.*29C>T