Canonical Allele Identifier: CA1149075042
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665663A= , CM000663.2:g.172665663A= GRCh38
NC_000001.10:g.172634803A= , CM000663.1:g.172634803A= GRCh37
NC_000001.9:g.170901426A= NCBI36
NG_007269.1:g.11619A= , LRG_58:g.11619A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.493A= MANE Select ENSP00000356694.2:p.Thr165=
ENST00000340030.4:c.*63A= ENSP00000344739.3:n.*63A=
ENST00000367721.2:c.493A= ENSP00000356694.2:p.Thr165=
NM_000639.2:c.493A= NP_000630.1:p.Thr165=
NM_001302746.1:c.*63A= NP_001289675.1:n.*63A=
NM_000639.3:c.493A= MANE Select NP_000630.1:p.Thr165=
NM_001302746.2:c.*63A= NP_001289675.1:n.*63A=
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