Canonical Allele Identifier: CA1144030463
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665749C= , CM000663.2:g.172665749C= GRCh38
NC_000001.10:g.172634889C= , CM000663.1:g.172634889C= GRCh37
NC_000001.9:g.170901512C= NCBI36
NG_007269.1:g.11705C= , LRG_58:g.11705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.579C= MANE Select ENSP00000356694.2:p.Ser193=
ENST00000340030.4:c.*149C= ENSP00000344739.3:n.*149C=
ENST00000367721.2:c.579C= ENSP00000356694.2:p.Ser193=
NM_000639.2:c.579C= NP_000630.1:p.Ser193=
NM_001302746.1:c.*149C= NP_001289675.1:n.*149C=
NM_000639.3:c.579C= MANE Select NP_000630.1:p.Ser193=
NM_001302746.2:c.*149C= NP_001289675.1:n.*149C=
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