Canonical Allele Identifier: CA383029999
Gene: SC5D HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.121177941C>A (hg19) chr11:g.121307232C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121307232C>A , CM000673.2:g.121307232C>A GRCh38
NC_000011.9:g.121177941C>A , CM000673.1:g.121177941C>A GRCh37
NC_000011.8:g.120683151C>A NCBI36
NG_009446.1:g.19554C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264027.9:c.620C>A MANE Select ENSP00000264027.4:p.Ser207Tyr
ENST00000264027.8:c.620C>A ENSP00000264027.4:p.Ser207Tyr
ENST00000392789.2:c.620C>A ENSP00000376539.2:p.Ser207Tyr
ENST00000527183.1:n.913C>A
ENST00000528991.1:n.313C>A
ENST00000534230.5:c.620C>A ENSP00000432550.1:p.Ser207Tyr
NM_001024956.2:c.620C>A NP_001020127.1:p.Ser207Tyr
NM_006918.4:c.620C>A NP_008849.2:p.Ser207Tyr
NM_006918.5:c.620C>A MANE Select NP_008849.2:p.Ser207Tyr
NM_001024956.3:c.620C>A NP_001020127.1:p.Ser207Tyr
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