Canonical Allele Identifier: CA383026304
Gene: SC5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121303524C>G , CM000673.2:g.121303524C>G GRCh38
NC_000011.9:g.121174233C>G , CM000673.1:g.121174233C>G GRCh37
NC_000011.8:g.120679443C>G NCBI36
NG_009446.1:g.15846C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264027.9:c.149C>G MANE Select ENSP00000264027.4:p.Ala50Gly
ENST00000264027.8:c.149C>G ENSP00000264027.4:p.Ala50Gly
ENST00000392789.2:c.149C>G ENSP00000376539.2:p.Ala50Gly
ENST00000524683.5:n.205C>G
ENST00000527762.5:c.149C>G ENSP00000436290.1:p.Ala50Gly
ENST00000531140.1:n.217C>G
ENST00000534230.5:c.149C>G ENSP00000432550.1:p.Ala50Gly
ENST00000534455.5:n.295C>G
NM_001024956.2:c.149C>G NP_001020127.1:p.Ala50Gly
NM_006918.4:c.149C>G NP_008849.2:p.Ala50Gly
NM_006918.5:c.149C>G MANE Select NP_008849.2:p.Ala50Gly
NM_001024956.3:c.149C>G NP_001020127.1:p.Ala50Gly