Canonical Allele Identifier: CA343805933
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665645-C-A
MyVariant Identifiers: chr1:g.172634785C>A (hg19) chr1:g.172665645C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665645C>A , CM000663.2:g.172665645C>A GRCh38
NC_000001.10:g.172634785C>A , CM000663.1:g.172634785C>A GRCh37
NC_000001.9:g.170901408C>A NCBI36
NG_007269.1:g.11601C>A , LRG_58:g.11601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.475C>A MANE Select ENSP00000356694.2:p.Pro159Thr
ENST00000340030.4:c.*45C>A ENSP00000344739.3:n.*45C>A
ENST00000367721.2:c.475C>A ENSP00000356694.2:p.Pro159Thr
NM_000639.2:c.475C>A NP_000630.1:p.Pro159Thr
NM_001302746.1:c.*45C>A NP_001289675.1:n.*45C>A
NM_000639.3:c.475C>A MANE Select NP_000630.1:p.Pro159Thr
NM_001302746.2:c.*45C>A NP_001289675.1:n.*45C>A
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