Canonical Allele Identifier: CA1593860624

Gene: SGCD

Linked Data

• dbSNP Id: rs1757601103

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766899_156766902dup , CM000667.2:g.156766899_156766902dup	GRCh38
NC_000005.9:g.156193910_156193913dup , CM000667.1:g.156193910_156193913dup	GRCh37
NC_000005.8:g.156126488_156126491dup	NCBI36
NG_008693.2:g.901557_901560dup , LRG_205:g.901557_901560dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.*7509_*7512dup MANE Select	ENSP00000338343.4:n.*7509_*7512dup
ENST00000435422.7:c.*7509_*7512dup	ENSP00000403003.2:n.*7509_*7512dup
NM_000337.5:c.*7509_*7512dup , LRG_205t1:c.*7509_*7512dup	NP_000328.2:n.*7509_*7512dup
NM_001128209.1:c.*7509_*7512dup	NP_001121681.1:n.*7509_*7512dup
XM_005265966.3:c.*7509_*7512dup	XP_005266023.1:n.*7509_*7512dup
XM_006714911.2:c.*7509_*7512dup	XP_006714974.1:n.*7509_*7512dup
XM_011534621.1:c.*7509_*7512dup	XP_011532923.1:n.*7509_*7512dup
NM_001128209.2:c.*7509_*7512dup	NP_001121681.1:n.*7509_*7512dup
NM_000337.6:c.*7509_*7512dup MANE Select	NP_000328.2:n.*7509_*7512dup