Canonical Allele Identifier: CA213249168

Gene: SMC3

Linked Data

• dbSNP Id: rs36066882
• MyVariant Identifiers: chr10:g.112361444_112361445insC (hg19) ; chr10:g.110601686_110601687insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110601686_110601687insC , CM000672.2:g.110601686_110601687insC	GRCh38
NC_000010.10:g.112361444_112361445insC , CM000672.1:g.112361444_112361445insC	GRCh37
NC_000010.9:g.112351434_112351435insC	NCBI36
NG_012217.1:g.38996_38997insC , LRG_774:g.38996_38997insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.4927_4928insC
ENST00000685743.1:n.2402_2403insC
ENST00000686057.1:n.1045_1046insC
ENST00000689321.1:n.1657_1658insC
ENST00000689986.1:n.483_484insC
ENST00000361804.5:c.2694_2695insC MANE Select	ENSP00000354720.5:p.Lys899GlnfsTer20
ENST00000361804.4:c.2694_2695insC	ENSP00000354720.4:p.Lys899GlnfsTer20
NM_005445.3:c.2694_2695insC , LRG_774t1:c.2694_2695insC	NP_005436.1:p.Lys899GlnfsTer20
NM_005445.4:c.2694_2695insC MANE Select	NP_005436.1:p.Lys899GlnfsTer20