Canonical Allele Identifier: CA1593854576
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156755008C= , CM000667.2:g.156755008C= GRCh38
NC_000005.9:g.156182019C= , CM000667.1:g.156182019C= GRCh37
NC_000005.8:g.156114597C= NCBI36
NG_008693.2:g.889666C= , LRG_205:g.889666C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.576-2573C= MANE Select ENSP00000338343.4:n.576-2573C=
ENST00000337851.8:c.576-2573C= ENSP00000338343.4:n.576-2573C=
ENST00000435422.7:c.573-2573C= ENSP00000403003.2:n.573-2573C=
ENST00000517913.5:c.576-2573C= ENSP00000429378.1:n.576-2573C=
NM_000337.5:c.576-2573C= , LRG_205t1:c.576-2573C= NP_000328.2:n.576-2573C=
NM_001128209.1:c.573-2573C= NP_001121681.1:n.573-2573C=
NM_172244.2:c.576-2573C= NP_758447.1:n.576-2573C=
XM_005265966.3:c.576-2573C= XP_005266023.1:n.576-2573C=
XM_005265967.1:c.503-2573C= XP_005266024.1:n.503-2573C=
XM_006714911.2:c.576-2573C= XP_006714974.1:n.576-2573C=
XM_011534621.1:c.573-2573C= XP_011532923.1:n.573-2573C=
XM_005265966.5:c.576-2573C= XP_005266023.1:n.576-2573C=
XM_005265967.2:c.503-2573C= XP_005266024.1:n.503-2573C=
XM_011534621.2:c.573-2573C= XP_011532923.1:n.573-2573C=
XM_017009723.2:c.576-2573C= XP_016865212.1:n.576-2573C=
XM_017009724.1:c.576-2573C= XP_016865213.1:n.576-2573C=
NM_001128209.2:c.573-2573C= NP_001121681.1:n.573-2573C=
NM_172244.3:c.576-2573C= NP_758447.1:n.576-2573C=
NM_000337.6:c.576-2573C= MANE Select NP_000328.2:n.576-2573C=