Canonical Allele Identifier: CA1593738928
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1756816738

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508824_156508827dup , CM000667.2:g.156508824_156508827dup GRCh38
NC_000005.9:g.155935834_155935837dup , CM000667.1:g.155935834_155935837dup GRCh37
NC_000005.8:g.155868412_155868415dup NCBI36
NG_008693.2:g.643481_643484dup , LRG_205:g.643481_643484dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.294+122_294+125dup MANE Select ENSP00000338343.4:n.294+122_294+125dup
ENST00000337851.8:c.294+122_294+125dup ENSP00000338343.4:n.294+122_294+125dup
ENST00000435422.7:c.291+122_291+125dup ENSP00000403003.2:n.291+122_291+125dup
ENST00000517913.5:c.294+122_294+125dup ENSP00000429378.1:n.294+122_294+125dup
ENST00000524347.2:c.*158+122_*158+125dup ENSP00000430794.1:n.*158+122_*158+125dup
NM_000337.5:c.294+122_294+125dup , LRG_205t1:c.294+122_294+125dup NP_000328.2:n.294+122_294+125dup
NM_001128209.1:c.291+122_291+125dup NP_001121681.1:n.291+122_291+125dup
NM_172244.2:c.294+122_294+125dup NP_758447.1:n.294+122_294+125dup
XM_005265966.3:c.294+122_294+125dup XP_005266023.1:n.294+122_294+125dup
XM_005265967.1:c.294+122_294+125dup XP_005266024.1:n.294+122_294+125dup
XM_006714911.2:c.294+122_294+125dup XP_006714974.1:n.294+122_294+125dup
XM_011534621.1:c.291+122_291+125dup XP_011532923.1:n.291+122_291+125dup
XM_005265966.5:c.294+122_294+125dup XP_005266023.1:n.294+122_294+125dup
XM_005265967.2:c.294+122_294+125dup XP_005266024.1:n.294+122_294+125dup
XM_011534621.2:c.291+122_291+125dup XP_011532923.1:n.291+122_291+125dup
XM_017009723.2:c.294+122_294+125dup XP_016865212.1:n.294+122_294+125dup
XM_017009724.1:c.294+122_294+125dup XP_016865213.1:n.294+122_294+125dup
NM_001128209.2:c.291+122_291+125dup NP_001121681.1:n.291+122_291+125dup
NM_172244.3:c.294+122_294+125dup NP_758447.1:n.294+122_294+125dup
NM_000337.6:c.294+122_294+125dup MANE Select NP_000328.2:n.294+122_294+125dup