Canonical Allele Identifier: CA1207431703
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665832A= , CM000663.2:g.172665832A= GRCh38
NC_000001.10:g.172634972A= , CM000663.1:g.172634972A= GRCh37
NC_000001.9:g.170901595A= NCBI36
NG_007269.1:g.11788A= , LRG_58:g.11788A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.662A= MANE Select ENSP00000356694.2:p.Asp221=
ENST00000340030.4:c.*232A= ENSP00000344739.3:n.*232A=
ENST00000367721.2:c.662A= ENSP00000356694.2:p.Asp221=
NM_000639.2:c.662A= NP_000630.1:p.Asp221=
NM_001302746.1:c.*232A= NP_001289675.1:n.*232A=
NM_000639.3:c.662A= MANE Select NP_000630.1:p.Asp221=
NM_001302746.2:c.*232A= NP_001289675.1:n.*232A=
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