Canonical Allele Identifier: CA2739272765
Gene: SGCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156594920_156594921insCCTCTCT , CM000667.2:g.156594920_156594921insCCTCTCT GRCh38
NC_000005.9:g.156021930_156021931insCCTCTCT , CM000667.1:g.156021930_156021931insCCTCTCT GRCh37
NC_000005.8:g.155954508_155954509insCCTCTCT NCBI36
NG_008693.2:g.729577_729578insCCTCTCT , LRG_205:g.729577_729578insCCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.383-12_383-11insCCTCTCT MANE Select ENSP00000338343.4:n.383-12_383-11insCCTCTCT
ENST00000337851.8:c.383-12_383-11insCCTCTCT ENSP00000338343.4:n.383-12_383-11insCCTCTCT
ENST00000435422.7:c.380-12_380-11insCCTCTCT ENSP00000403003.2:n.380-12_380-11insCCTCTCT
ENST00000517913.5:c.383-12_383-11insCCTCTCT ENSP00000429378.1:n.383-12_383-11insCCTCTCT
NM_000337.5:c.383-12_383-11insCCTCTCT , LRG_205t1:c.383-12_383-11insCCTCTCT NP_000328.2:n.383-12_383-11insCCTCTCT
NM_001128209.1:c.380-12_380-11insCCTCTCT NP_001121681.1:n.380-12_380-11insCCTCTCT
NM_172244.2:c.383-12_383-11insCCTCTCT NP_758447.1:n.383-12_383-11insCCTCTCT
XM_005265966.3:c.383-12_383-11insCCTCTCT XP_005266023.1:n.383-12_383-11insCCTCTCT
XM_005265967.1:c.383-12_383-11insCCTCTCT XP_005266024.1:n.383-12_383-11insCCTCTCT
XM_006714911.2:c.383-12_383-11insCCTCTCT XP_006714974.1:n.383-12_383-11insCCTCTCT
XM_011534621.1:c.380-12_380-11insCCTCTCT XP_011532923.1:n.380-12_380-11insCCTCTCT
XM_005265966.5:c.383-12_383-11insCCTCTCT XP_005266023.1:n.383-12_383-11insCCTCTCT
XM_005265967.2:c.383-12_383-11insCCTCTCT XP_005266024.1:n.383-12_383-11insCCTCTCT
XM_011534621.2:c.380-12_380-11insCCTCTCT XP_011532923.1:n.380-12_380-11insCCTCTCT
XM_017009723.2:c.383-12_383-11insCCTCTCT XP_016865212.1:n.383-12_383-11insCCTCTCT
XM_017009724.1:c.383-12_383-11insCCTCTCT XP_016865213.1:n.383-12_383-11insCCTCTCT
NM_001128209.2:c.380-12_380-11insCCTCTCT NP_001121681.1:n.380-12_380-11insCCTCTCT
NM_172244.3:c.383-12_383-11insCCTCTCT NP_758447.1:n.383-12_383-11insCCTCTCT
NM_000337.6:c.383-12_383-11insCCTCTCT MANE Select NP_000328.2:n.383-12_383-11insCCTCTCT