Canonical Allele Identifier: CA1148451381
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665715T= , CM000663.2:g.172665715T= GRCh38
NC_000001.10:g.172634855T= , CM000663.1:g.172634855T= GRCh37
NC_000001.9:g.170901478T= NCBI36
NG_007269.1:g.11671T= , LRG_58:g.11671T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.545T= MANE Select ENSP00000356694.2:p.Val182=
ENST00000340030.4:c.*115T= ENSP00000344739.3:n.*115T=
ENST00000367721.2:c.545T= ENSP00000356694.2:p.Val182=
NM_000639.2:c.545T= NP_000630.1:p.Val182=
NM_001302746.1:c.*115T= NP_001289675.1:n.*115T=
NM_000639.3:c.545T= MANE Select NP_000630.1:p.Val182=
NM_001302746.2:c.*115T= NP_001289675.1:n.*115T=
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