Canonical Allele Identifier: CA2646937019
Gene: SYPL2 HGNC NCBI

Linked Data

gnomAD v4: 1-109480813-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109480813C>A , CM000663.2:g.109480813C>A GRCh38
NC_000001.10:g.110023435C>A , CM000663.1:g.110023435C>A GRCh37
NC_000001.9:g.109824958C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369872.4:c.*1265C>A MANE Select ENSP00000358888.3:n.*1265C>A
ENST00000369872.3:c.*1265C>A ENSP00000358888.3:n.*1265C>A
NM_001040709.1:c.*1265C>A NP_001035799.1:n.*1265C>A
XM_011541285.1:c.*1265C>A XP_011539587.1:n.*1265C>A
NM_001040709.2:c.*1265C>A MANE Select NP_001035799.1:n.*1265C>A
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