Canonical Allele Identifier: CA413255607

Gene: SMC1A

Linked Data

• dbSNP Id: rs2075702006
• MyVariant Identifiers: chrX:g.53436112C>T (hg19) ; chrX:g.53409181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53409181C>T , CM000685.2:g.53409181C>T	GRCh38
NC_000023.10:g.53436112C>T , CM000685.1:g.53436112C>T	GRCh37
NC_000023.9:g.53452837C>T	NCBI36
NG_006988.2:g.18490G>A , LRG_773:g.18490G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1426G>A MANE Select	ENSP00000323421.3:p.Glu476Lys
ENST00000674590.1:c.658G>A	ENSP00000502626.1:p.Glu220Lys
ENST00000675065.1:n.778G>A
ENST00000675504.1:c.1360G>A	ENSP00000502524.1:p.Glu454Lys
ENST00000322213.8:c.1426G>A	ENSP00000323421.3:p.Glu476Lys
ENST00000375340.10:c.1360G>A	ENSP00000364489.7:p.Glu454Lys
NM_001281463.1:c.1360G>A , LRG_773t1:c.1360G>A	NP_001268392.1:p.Glu454Lys
NM_006306.3:c.1426G>A , LRG_773t2:c.1426G>A	NP_006297.2:p.Glu476Lys
NM_006306.4:c.1426G>A MANE Select	NP_006297.2:p.Glu476Lys