Canonical Allele Identifier: CA2004808915
Gene: SC5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121303526A= , CM000673.2:g.121303526A= GRCh38
NC_000011.9:g.121174235A= , CM000673.1:g.121174235A= GRCh37
NC_000011.8:g.120679445A= NCBI36
NG_009446.1:g.15848A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264027.9:c.151A= MANE Select ENSP00000264027.4:p.Thr51=
ENST00000264027.8:c.151A= ENSP00000264027.4:p.Thr51=
ENST00000392789.2:c.151A= ENSP00000376539.2:p.Thr51=
ENST00000524683.5:n.207A=
ENST00000527762.5:c.151A= ENSP00000436290.1:p.Thr51=
ENST00000531140.1:n.219A=
ENST00000534230.5:c.151A= ENSP00000432550.1:p.Thr51=
ENST00000534455.5:n.297A=
NM_001024956.2:c.151A= NP_001020127.1:p.Thr51=
NM_006918.4:c.151A= NP_008849.2:p.Thr51=
NM_006918.5:c.151A= MANE Select NP_008849.2:p.Thr51=
NM_001024956.3:c.151A= NP_001020127.1:p.Thr51=