Canonical Allele Identifier: CA1083278741
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156344423_156344425dup , CM000667.2:g.156344423_156344425dup GRCh38
NC_000005.9:g.155771433_155771435dup , CM000667.1:g.155771433_155771435dup GRCh37
NC_000005.8:g.155704011_155704013dup NCBI36
NG_008693.2:g.479080_479082dup , LRG_205:g.479080_479082dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.4-66_4-64dup MANE Select ENSP00000338343.4:n.4-66_4-64dup
ENST00000337851.8:c.4-66_4-64dup ENSP00000338343.4:n.4-66_4-64dup
ENST00000435422.7:c.1-66_1-64dup ENSP00000403003.2:n.1-66_1-64dup
ENST00000517913.5:c.4-66_4-64dup ENSP00000429378.1:n.4-66_4-64dup
ENST00000524347.2:c.4-66_4-64dup ENSP00000430794.1:n.4-66_4-64dup
NM_000337.5:c.4-66_4-64dup , LRG_205t1:c.4-66_4-64dup NP_000328.2:n.4-66_4-64dup
NM_001128209.1:c.1-66_1-64dup NP_001121681.1:n.1-66_1-64dup
NM_172244.2:c.4-66_4-64dup NP_758447.1:n.4-66_4-64dup
XM_005265966.3:c.4-66_4-64dup XP_005266023.1:n.4-66_4-64dup
XM_005265967.1:c.4-66_4-64dup XP_005266024.1:n.4-66_4-64dup
XM_006714911.2:c.4-66_4-64dup XP_006714974.1:n.4-66_4-64dup
XM_011534621.1:c.1-66_1-64dup XP_011532923.1:n.1-66_1-64dup
XR_941123.1:n.254+3028_254+3030dup
XM_005265966.5:c.4-66_4-64dup XP_005266023.1:n.4-66_4-64dup
XM_005265967.2:c.4-66_4-64dup XP_005266024.1:n.4-66_4-64dup
XM_011534621.2:c.1-66_1-64dup XP_011532923.1:n.1-66_1-64dup
XM_017009723.2:c.4-66_4-64dup XP_016865212.1:n.4-66_4-64dup
XM_017009724.1:c.4-66_4-64dup XP_016865213.1:n.4-66_4-64dup
NM_001128209.2:c.1-66_1-64dup NP_001121681.1:n.1-66_1-64dup
NM_172244.3:c.4-66_4-64dup NP_758447.1:n.4-66_4-64dup
NM_000337.6:c.4-66_4-64dup MANE Select NP_000328.2:n.4-66_4-64dup