Canonical Allele Identifier: CA659784780

Gene: SMC3

Linked Data

• dbSNP Id: rs1200835850
• gnomAD v3: 10-110581837-ATAATT-A
• gnomAD v4: 10-110581837-ATAATT-A
• MyVariant Identifiers: chr10:g.112341596_112341600del (hg19) ; chr10:g.110581838_110581842del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110581843_110581847del , CM000672.2:g.110581843_110581847del	GRCh38
NC_000010.10:g.112341601_112341605del , CM000672.1:g.112341601_112341605del	GRCh37
NC_000010.9:g.112331591_112331595del	NCBI36
NG_012217.1:g.19153_19157del , LRG_774:g.19153_19157del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684988.1:n.681-80_681-76del
ENST00000687823.1:n.462-80_462-76del
ENST00000689932.1:n.2611-80_2611-76del
ENST00000691297.1:n.681-80_681-76del
ENST00000691527.1:n.1351-80_1351-76del
ENST00000692792.1:n.667-80_667-76del
ENST00000361804.5:c.548-80_548-76del MANE Select	ENSP00000354720.5:n.548-80_548-76del
ENST00000361804.4:c.548-80_548-76del	ENSP00000354720.4:n.548-80_548-76del
ENST00000462899.1:n.694-80_694-76del
NM_005445.3:c.548-80_548-76del , LRG_774t1:c.548-80_548-76del	NP_005436.1:n.548-80_548-76del
NM_005445.4:c.548-80_548-76del MANE Select	NP_005436.1:n.548-80_548-76del