Canonical Allele Identifier: CA3530601
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 411706
dbSNP Id: rs752000538

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156595007A>G , CM000667.2:g.156595007A>G GRCh38
NC_000005.9:g.156022017A>G , CM000667.1:g.156022017A>G GRCh37
NC_000005.8:g.155954595A>G NCBI36
NG_008693.2:g.729664A>G , LRG_205:g.729664A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.458A>G MANE Select ENSP00000338343.4:p.Asp153Gly
ENST00000337851.8:c.458A>G ENSP00000338343.4:p.Asp153Gly
ENST00000435422.7:c.455A>G ENSP00000403003.2:p.Asp152Gly
ENST00000517913.5:c.458A>G ENSP00000429378.1:p.Asp153Gly
NM_000337.5:c.458A>G , LRG_205t1:c.458A>G NP_000328.2:p.Asp153Gly
NM_001128209.1:c.455A>G NP_001121681.1:p.Asp152Gly
NM_172244.2:c.458A>G NP_758447.1:p.Asp153Gly
XM_005265966.3:c.458A>G XP_005266023.1:p.Asp153Gly
XM_005265967.1:c.458A>G XP_005266024.1:p.Asp153Gly
XM_006714911.2:c.458A>G XP_006714974.1:p.Asp153Gly
XM_011534621.1:c.455A>G XP_011532923.1:p.Asp152Gly
XM_005265966.5:c.458A>G XP_005266023.1:p.Asp153Gly
XM_005265967.2:c.458A>G XP_005266024.1:p.Asp153Gly
XM_011534621.2:c.455A>G XP_011532923.1:p.Asp152Gly
XM_017009723.2:c.458A>G XP_016865212.1:p.Asp153Gly
XM_017009724.1:c.458A>G XP_016865213.1:p.Asp153Gly
NM_001128209.2:c.455A>G NP_001121681.1:p.Asp152Gly
NM_172244.3:c.458A>G NP_758447.1:p.Asp153Gly
NM_000337.6:c.458A>G MANE Select NP_000328.2:p.Asp153Gly