Canonical Allele Identifier: CA383030634
Gene: SC5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121307364G>T , CM000673.2:g.121307364G>T GRCh38
NC_000011.9:g.121178073G>T , CM000673.1:g.121178073G>T GRCh37
NC_000011.8:g.120683283G>T NCBI36
NG_009446.1:g.19686G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264027.9:c.752G>T MANE Select ENSP00000264027.4:p.Gly251Val
ENST00000264027.8:c.752G>T ENSP00000264027.4:p.Gly251Val
ENST00000392789.2:c.752G>T ENSP00000376539.2:p.Gly251Val
ENST00000527183.1:n.1045G>T
ENST00000534230.5:c.632-93G>T ENSP00000432550.1:n.632-93G>T
NM_001024956.2:c.752G>T NP_001020127.1:p.Gly251Val
NM_006918.4:c.752G>T NP_008849.2:p.Gly251Val
NM_006918.5:c.752G>T MANE Select NP_008849.2:p.Gly251Val
NM_001024956.3:c.752G>T NP_001020127.1:p.Gly251Val