Canonical Allele Identifier: CA659802645

Gene: SMC3

Linked Data

• dbSNP Id: rs1459418006
• MyVariant Identifiers: chr10:g.112361957_112361961del (hg19) ; chr10:g.110602199_110602203del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110602200_110602204del , CM000672.2:g.110602200_110602204del	GRCh38
NC_000010.10:g.112361958_112361962del , CM000672.1:g.112361958_112361962del	GRCh37
NC_000010.9:g.112351948_112351952del	NCBI36
NG_012217.1:g.39510_39514del , LRG_774:g.39510_39514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.5338+22_5338+26del
ENST00000685743.1:n.2813+22_2813+26del
ENST00000686057.1:n.1456+22_1456+26del
ENST00000689321.1:n.2068+22_2068+26del
ENST00000689986.1:n.894+22_894+26del
ENST00000361804.5:c.3105+22_3105+26del MANE Select	ENSP00000354720.5:n.3105+22_3105+26del
ENST00000361804.4:c.3105+22_3105+26del	ENSP00000354720.4:n.3105+22_3105+26del
NM_005445.3:c.3105+22_3105+26del , LRG_774t1:c.3105+22_3105+26del	NP_005436.1:n.3105+22_3105+26del
NM_005445.4:c.3105+22_3105+26del MANE Select	NP_005436.1:n.3105+22_3105+26del