Canonical Allele Identifier: CA477383899

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121178077C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121307368C>G , CM000673.2:g.121307368C>G	GRCh38
NC_000011.9:g.121178077C>G , CM000673.1:g.121178077C>G	GRCh37
NC_000011.8:g.120683287C>G	NCBI36
NG_009446.1:g.19690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.756C>G MANE Select	ENSP00000264027.4:p.Gly252=
ENST00000264027.8:c.756C>G	ENSP00000264027.4:p.Gly252=
ENST00000392789.2:c.756C>G	ENSP00000376539.2:p.Gly252=
ENST00000527183.1:n.1049C>G
ENST00000534230.5:c.632-89C>G	ENSP00000432550.1:n.632-89C>G
NM_001024956.2:c.756C>G	NP_001020127.1:p.Gly252=
NM_006918.4:c.756C>G	NP_008849.2:p.Gly252=
NM_006918.5:c.756C>G MANE Select	NP_008849.2:p.Gly252=
NM_001024956.3:c.756C>G	NP_001020127.1:p.Gly252=