Canonical Allele Identifier: CA378376289

Gene: SMC3

Linked Data

• COSMIC: COSM465251
• MyVariant Identifiers: chr10:g.112341762T>C (hg19) ; chr10:g.110582004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110582004T>C , CM000672.2:g.110582004T>C	GRCh38
NC_000010.10:g.112341762T>C , CM000672.1:g.112341762T>C	GRCh37
NC_000010.9:g.112331752T>C	NCBI36
NG_012217.1:g.19314T>C , LRG_774:g.19314T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.762T>C
ENST00000687823.1:n.543T>C
ENST00000689932.1:n.2692T>C
ENST00000691297.1:n.762T>C
ENST00000691527.1:n.1432T>C
ENST00000692792.1:n.748T>C
ENST00000361804.5:c.629T>C MANE Select	ENSP00000354720.5:p.Leu210Pro
ENST00000361804.4:c.629T>C	ENSP00000354720.4:p.Leu210Pro
ENST00000462899.1:n.775T>C
NM_005445.3:c.629T>C , LRG_774t1:c.629T>C	NP_005436.1:p.Leu210Pro
NM_005445.4:c.629T>C MANE Select	NP_005436.1:p.Leu210Pro