Canonical Allele Identifier: CA2610888186

Gene: SMC3

Linked Data

• gnomAD v4: 10-110601956-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601957del , CM000672.2:g.110601957del	GRCh38
NC_000010.10:g.112361715del , CM000672.1:g.112361715del	GRCh37
NC_000010.9:g.112351705del	NCBI36
NG_012217.1:g.39267del , LRG_774:g.39267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.5126-9del
ENST00000685743.1:n.2601-9del
ENST00000686057.1:n.1244-9del
ENST00000689321.1:n.1856-9del
ENST00000689986.1:n.682-9del
ENST00000361804.5:c.2893-9del MANE Select	ENSP00000354720.5:n.2893-9del
ENST00000361804.4:c.2893-9del	ENSP00000354720.4:n.2893-9del
NM_005445.3:c.2893-9del , LRG_774t1:c.2893-9del	NP_005436.1:n.2893-9del
NM_005445.4:c.2893-9del MANE Select	NP_005436.1:n.2893-9del