Canonical Allele Identifier: CA650706065

Gene: SGCD

Linked Data

• COSMIC: COSN21712395

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766963_156766964insT , CM000667.2:g.156766963_156766964insT	GRCh38
NC_000005.9:g.156193974_156193975insT , CM000667.1:g.156193974_156193975insT	GRCh37
NC_000005.8:g.156126552_156126553insT	NCBI36
NG_008693.2:g.901621_901622insT , LRG_205:g.901621_901622insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.*7573_*7574insT MANE Select	ENSP00000338343.4:n.*7573_*7574insT
ENST00000435422.7:c.*7573_*7574insT	ENSP00000403003.2:n.*7573_*7574insT
NM_000337.5:c.*7573_*7574insT , LRG_205t1:c.*7573_*7574insT	NP_000328.2:n.*7573_*7574insT
NM_001128209.1:c.*7573_*7574insT	NP_001121681.1:n.*7573_*7574insT
XM_005265966.3:c.*7573_*7574insT	XP_005266023.1:n.*7573_*7574insT
XM_006714911.2:c.*7573_*7574insT	XP_006714974.1:n.*7573_*7574insT
XM_011534621.1:c.*7573_*7574insT	XP_011532923.1:n.*7573_*7574insT
NM_001128209.2:c.*7573_*7574insT	NP_001121681.1:n.*7573_*7574insT
NM_000337.6:c.*7573_*7574insT MANE Select	NP_000328.2:n.*7573_*7574insT