Canonical Allele Identifier: CA1593804985
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156647261_156647263delinsAAG , CM000667.2:g.156647261_156647263delinsAAG GRCh38
NC_000005.9:g.156074271_156074273delinsAAG , CM000667.1:g.156074271_156074273delinsAAG GRCh37
NC_000005.8:g.156006849_156006851delinsAAG NCBI36
NG_008693.2:g.781918_781920delinsAAG , LRG_205:g.781918_781920delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.503-203_503-201delinsAAG MANE Select ENSP00000338343.4:n.503-203_503-201delinsAAG
ENST00000337851.8:c.503-203_503-201delinsAAG ENSP00000338343.4:n.503-203_503-201delinsAAG
ENST00000435422.7:c.500-203_500-201delinsAAG ENSP00000403003.2:n.500-203_500-201delinsAAG
ENST00000517913.5:c.503-203_503-201delinsAAG ENSP00000429378.1:n.503-203_503-201delinsAAG
NM_000337.5:c.503-203_503-201delinsAAG , LRG_205t1:c.503-203_503-201delinsAAG NP_000328.2:n.503-203_503-201delinsAAG
NM_001128209.1:c.500-203_500-201delinsAAG NP_001121681.1:n.500-203_500-201delinsAAG
NM_172244.2:c.503-203_503-201delinsAAG NP_758447.1:n.503-203_503-201delinsAAG
XM_005265966.3:c.503-203_503-201delinsAAG XP_005266023.1:n.503-203_503-201delinsAAG
XM_005265967.1:c.502+52210_502+52212delinsAAG XP_005266024.1:n.502+52210_502+52212delinsAAG
XM_006714911.2:c.503-203_503-201delinsAAG XP_006714974.1:n.503-203_503-201delinsAAG
XM_011534621.1:c.500-203_500-201delinsAAG XP_011532923.1:n.500-203_500-201delinsAAG
XM_005265966.5:c.503-203_503-201delinsAAG XP_005266023.1:n.503-203_503-201delinsAAG
XM_005265967.2:c.502+52210_502+52212delinsAAG XP_005266024.1:n.502+52210_502+52212delinsAAG
XM_011534621.2:c.500-203_500-201delinsAAG XP_011532923.1:n.500-203_500-201delinsAAG
XM_017009723.2:c.503-203_503-201delinsAAG XP_016865212.1:n.503-203_503-201delinsAAG
XM_017009724.1:c.503-203_503-201delinsAAG XP_016865213.1:n.503-203_503-201delinsAAG
NM_001128209.2:c.500-203_500-201delinsAAG NP_001121681.1:n.500-203_500-201delinsAAG
NM_172244.3:c.503-203_503-201delinsAAG NP_758447.1:n.503-203_503-201delinsAAG
NM_000337.6:c.503-203_503-201delinsAAG MANE Select NP_000328.2:n.503-203_503-201delinsAAG