Canonical Allele Identifier: CA806165609
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1323377587

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156509062_156509063del , CM000667.2:g.156509062_156509063del GRCh38
NC_000005.9:g.155936072_155936073del , CM000667.1:g.155936072_155936073del GRCh37
NC_000005.8:g.155868650_155868651del NCBI36
NG_008693.2:g.643719_643720del , LRG_205:g.643719_643720del

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.294+360_294+361del MANE Select ENSP00000338343.4:n.294+360_294+361del
ENST00000337851.8:c.294+360_294+361del ENSP00000338343.4:n.294+360_294+361del
ENST00000435422.7:c.291+360_291+361del ENSP00000403003.2:n.291+360_291+361del
ENST00000517913.5:c.294+360_294+361del ENSP00000429378.1:n.294+360_294+361del
ENST00000524347.2:c.*158+360_*158+361del ENSP00000430794.1:n.*158+360_*158+361del
NM_000337.5:c.294+360_294+361del , LRG_205t1:c.294+360_294+361del NP_000328.2:n.294+360_294+361del
NM_001128209.1:c.291+360_291+361del NP_001121681.1:n.291+360_291+361del
NM_172244.2:c.294+360_294+361del NP_758447.1:n.294+360_294+361del
XM_005265966.3:c.294+360_294+361del XP_005266023.1:n.294+360_294+361del
XM_005265967.1:c.294+360_294+361del XP_005266024.1:n.294+360_294+361del
XM_006714911.2:c.294+360_294+361del XP_006714974.1:n.294+360_294+361del
XM_011534621.1:c.291+360_291+361del XP_011532923.1:n.291+360_291+361del
XM_005265966.5:c.294+360_294+361del XP_005266023.1:n.294+360_294+361del
XM_005265967.2:c.294+360_294+361del XP_005266024.1:n.294+360_294+361del
XM_011534621.2:c.291+360_291+361del XP_011532923.1:n.291+360_291+361del
XM_017009723.2:c.294+360_294+361del XP_016865212.1:n.294+360_294+361del
XM_017009724.1:c.294+360_294+361del XP_016865213.1:n.294+360_294+361del
NM_001128209.2:c.291+360_291+361del NP_001121681.1:n.291+360_291+361del
NM_172244.3:c.294+360_294+361del NP_758447.1:n.294+360_294+361del
NM_000337.6:c.294+360_294+361del MANE Select NP_000328.2:n.294+360_294+361del