Canonical Allele Identifier: CA2610888396

Gene: SMC3

Linked Data

• gnomAD v4: 10-110602188-GCTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110602189_110602192del , CM000672.2:g.110602189_110602192del	GRCh38
NC_000010.10:g.112361947_112361950del , CM000672.1:g.112361947_112361950del	GRCh37
NC_000010.9:g.112351937_112351940del	NCBI36
NG_012217.1:g.39499_39502del , LRG_774:g.39499_39502del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684988.1:n.5338+11_5338+14del
ENST00000685743.1:n.2813+11_2813+14del
ENST00000686057.1:n.1456+11_1456+14del
ENST00000689321.1:n.2068+11_2068+14del
ENST00000689986.1:n.894+11_894+14del
ENST00000361804.5:c.3105+11_3105+14del MANE Select	ENSP00000354720.5:n.3105+11_3105+14del
ENST00000361804.4:c.3105+11_3105+14del	ENSP00000354720.4:n.3105+11_3105+14del
NM_005445.3:c.3105+11_3105+14del , LRG_774t1:c.3105+11_3105+14del	NP_005436.1:n.3105+11_3105+14del
NM_005445.4:c.3105+11_3105+14del MANE Select	NP_005436.1:n.3105+11_3105+14del