Canonical Allele Identifier: CA383029275
Gene: SC5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121307114T>G , CM000673.2:g.121307114T>G GRCh38
NC_000011.9:g.121177823T>G , CM000673.1:g.121177823T>G GRCh37
NC_000011.8:g.120683033T>G NCBI36
NG_009446.1:g.19436T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264027.9:c.502T>G MANE Select ENSP00000264027.4:p.Phe168Val
ENST00000264027.8:c.502T>G ENSP00000264027.4:p.Phe168Val
ENST00000392789.2:c.502T>G ENSP00000376539.2:p.Phe168Val
ENST00000527183.1:n.795T>G
ENST00000527762.5:c.523T>G ENSP00000436290.1:p.Phe175Val
ENST00000528991.1:n.195T>G
ENST00000534230.5:c.502T>G ENSP00000432550.1:p.Phe168Val
NM_001024956.2:c.502T>G NP_001020127.1:p.Phe168Val
NM_006918.4:c.502T>G NP_008849.2:p.Phe168Val
NM_006918.5:c.502T>G MANE Select NP_008849.2:p.Phe168Val
NM_001024956.3:c.502T>G NP_001020127.1:p.Phe168Val