Canonical Allele Identifier: CA1083278731
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1768832266

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156344413_156344414insG , CM000667.2:g.156344413_156344414insG GRCh38
NC_000005.9:g.155771423_155771424insG , CM000667.1:g.155771423_155771424insG GRCh37
NC_000005.8:g.155704001_155704002insG NCBI36
NG_008693.2:g.479070_479071insG , LRG_205:g.479070_479071insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.4-76_4-75insG MANE Select ENSP00000338343.4:n.4-76_4-75insG
ENST00000337851.8:c.4-76_4-75insG ENSP00000338343.4:n.4-76_4-75insG
ENST00000435422.7:c.1-76_1-75insG ENSP00000403003.2:n.1-76_1-75insG
ENST00000517913.5:c.4-76_4-75insG ENSP00000429378.1:n.4-76_4-75insG
ENST00000524347.2:c.4-76_4-75insG ENSP00000430794.1:n.4-76_4-75insG
NM_000337.5:c.4-76_4-75insG , LRG_205t1:c.4-76_4-75insG NP_000328.2:n.4-76_4-75insG
NM_001128209.1:c.1-76_1-75insG NP_001121681.1:n.1-76_1-75insG
NM_172244.2:c.4-76_4-75insG NP_758447.1:n.4-76_4-75insG
XM_005265966.3:c.4-76_4-75insG XP_005266023.1:n.4-76_4-75insG
XM_005265967.1:c.4-76_4-75insG XP_005266024.1:n.4-76_4-75insG
XM_006714911.2:c.4-76_4-75insG XP_006714974.1:n.4-76_4-75insG
XM_011534621.1:c.1-76_1-75insG XP_011532923.1:n.1-76_1-75insG
XR_941123.1:n.254+3039_254+3040insC
XM_005265966.5:c.4-76_4-75insG XP_005266023.1:n.4-76_4-75insG
XM_005265967.2:c.4-76_4-75insG XP_005266024.1:n.4-76_4-75insG
XM_011534621.2:c.1-76_1-75insG XP_011532923.1:n.1-76_1-75insG
XM_017009723.2:c.4-76_4-75insG XP_016865212.1:n.4-76_4-75insG
XM_017009724.1:c.4-76_4-75insG XP_016865213.1:n.4-76_4-75insG
NM_001128209.2:c.1-76_1-75insG NP_001121681.1:n.1-76_1-75insG
NM_172244.3:c.4-76_4-75insG NP_758447.1:n.4-76_4-75insG
NM_000337.6:c.4-76_4-75insG MANE Select NP_000328.2:n.4-76_4-75insG