Canonical Allele Identifier: CA1207431663
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665698_172665701delinsTAAG , CM000663.2:g.172665698_172665701delinsTAAG GRCh38
NC_000001.10:g.172634838_172634841delinsTAAG , CM000663.1:g.172634838_172634841delinsTAAG GRCh37
NC_000001.9:g.170901461_170901464delinsTAAG NCBI36
NG_007269.1:g.11654_11657delinsTAAG , LRG_58:g.11654_11657delinsTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.528_531delinsTAAG MANE Select ENSP00000356694.2:p.Tyr176=
ENST00000340030.4:c.*98_*101delinsTAAG ENSP00000344739.3:n.*98_*101delinsTAAG
ENST00000367721.2:c.528_531delinsTAAG ENSP00000356694.2:p.Tyr176=
NM_000639.2:c.528_531delinsTAAG NP_000630.1:p.Tyr176=
NM_001302746.1:c.*98_*101delinsTAAG NP_001289675.1:n.*98_*101delinsTAAG
NM_000639.3:c.528_531delinsTAAG MANE Select NP_000630.1:p.Tyr176=
NM_001302746.2:c.*98_*101delinsTAAG NP_001289675.1:n.*98_*101delinsTAAG
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