Canonical Allele Identifier: CA1593779062
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs138491950

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156594888_156594891dup , CM000667.2:g.156594888_156594891dup GRCh38
NC_000005.9:g.156021898_156021901dup , CM000667.1:g.156021898_156021901dup GRCh37
NC_000005.8:g.155954476_155954479dup NCBI36
NG_008693.2:g.729545_729548dup , LRG_205:g.729545_729548dup

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.383-44_383-41dup MANE Select ENSP00000338343.4:n.383-44_383-41dup
ENST00000337851.8:c.383-44_383-41dup ENSP00000338343.4:n.383-44_383-41dup
ENST00000435422.7:c.380-44_380-41dup ENSP00000403003.2:n.380-44_380-41dup
ENST00000517913.5:c.383-44_383-41dup ENSP00000429378.1:n.383-44_383-41dup
NM_000337.5:c.383-44_383-41dup , LRG_205t1:c.383-44_383-41dup NP_000328.2:n.383-44_383-41dup
NM_001128209.1:c.380-44_380-41dup NP_001121681.1:n.380-44_380-41dup
NM_172244.2:c.383-44_383-41dup NP_758447.1:n.383-44_383-41dup
XM_005265966.3:c.383-44_383-41dup XP_005266023.1:n.383-44_383-41dup
XM_005265967.1:c.383-44_383-41dup XP_005266024.1:n.383-44_383-41dup
XM_006714911.2:c.383-44_383-41dup XP_006714974.1:n.383-44_383-41dup
XM_011534621.1:c.380-44_380-41dup XP_011532923.1:n.380-44_380-41dup
XM_005265966.5:c.383-44_383-41dup XP_005266023.1:n.383-44_383-41dup
XM_005265967.2:c.383-44_383-41dup XP_005266024.1:n.383-44_383-41dup
XM_011534621.2:c.380-44_380-41dup XP_011532923.1:n.380-44_380-41dup
XM_017009723.2:c.383-44_383-41dup XP_016865212.1:n.383-44_383-41dup
XM_017009724.1:c.383-44_383-41dup XP_016865213.1:n.383-44_383-41dup
NM_001128209.2:c.380-44_380-41dup NP_001121681.1:n.380-44_380-41dup
NM_172244.3:c.383-44_383-41dup NP_758447.1:n.383-44_383-41dup
NM_000337.6:c.383-44_383-41dup MANE Select NP_000328.2:n.383-44_383-41dup