Canonical Allele Identifier: CA1207431677
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665734G= , CM000663.2:g.172665734G= GRCh38
NC_000001.10:g.172634874G= , CM000663.1:g.172634874G= GRCh37
NC_000001.9:g.170901497G= NCBI36
NG_007269.1:g.11690G= , LRG_58:g.11690G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.564G= MANE Select ENSP00000356694.2:p.Leu188=
ENST00000340030.4:c.*134G= ENSP00000344739.3:n.*134G=
ENST00000367721.2:c.564G= ENSP00000356694.2:p.Leu188=
NM_000639.2:c.564G= NP_000630.1:p.Leu188=
NM_001302746.1:c.*134G= NP_001289675.1:n.*134G=
NM_000639.3:c.564G= MANE Select NP_000630.1:p.Leu188=
NM_001302746.2:c.*134G= NP_001289675.1:n.*134G=
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