Canonical Allele Identifier: CA413255441

Gene: SMC1A

Linked Data

• ClinVar Variation Id: 489224
• ClinVar RCV Id: RCV000578696 ; RCV001270901 ; RCV001387822
• dbSNP Id: rs1556890135
• MyVariant Identifiers: chrX:g.53436043G>A (hg19) ; chrX:g.53409112G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53409112G>A , CM000685.2:g.53409112G>A	GRCh38
NC_000023.10:g.53436043G>A , CM000685.1:g.53436043G>A	GRCh37
NC_000023.9:g.53452768G>A	NCBI36
NG_006988.2:g.18559C>T , LRG_773:g.18559C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322213.9:c.1495C>T MANE Select	ENSP00000323421.3:p.Arg499Ter
ENST00000674590.1:c.727C>T	ENSP00000502626.1:p.Arg243Ter
ENST00000675065.1:n.847C>T
ENST00000675504.1:c.1429C>T	ENSP00000502524.1:p.Arg477Ter
ENST00000322213.8:c.1495C>T	ENSP00000323421.3:p.Arg499Ter
ENST00000375340.10:c.1429C>T	ENSP00000364489.7:p.Arg477Ter
NM_001281463.1:c.1429C>T , LRG_773t1:c.1429C>T	NP_001268392.1:p.Arg477Ter
NM_006306.3:c.1495C>T , LRG_773t2:c.1495C>T	NP_006297.2:p.Arg499Ter
NM_006306.4:c.1495C>T MANE Select	NP_006297.2:p.Arg499Ter