Canonical Allele Identifier: CA329907442

Gene: SMC1A

Linked Data

• dbSNP Id: rs371494870
• gnomAD v3: X-53409055-C-A
• gnomAD v4: X-53409055-C-A
• MyVariant Identifiers: chrX:g.53435986C>A (hg19) ; chrX:g.53409055C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53409055C>A , CM000685.2:g.53409055C>A	GRCh38
NC_000023.10:g.53435986C>A , CM000685.1:g.53435986C>A	GRCh37
NC_000023.9:g.53452711C>A	NCBI36
NG_006988.2:g.18616G>T , LRG_773:g.18616G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1545+7G>T MANE Select	ENSP00000323421.3:n.1545+7G>T
ENST00000674590.1:c.777+7G>T	ENSP00000502626.1:n.777+7G>T
ENST00000675065.1:n.897+7G>T
ENST00000675504.1:c.1479+7G>T	ENSP00000502524.1:n.1479+7G>T
ENST00000322213.8:c.1545+7G>T	ENSP00000323421.3:n.1545+7G>T
ENST00000375340.10:c.1479+7G>T	ENSP00000364489.7:n.1479+7G>T
NM_001281463.1:c.1479+7G>T , LRG_773t1:c.1479+7G>T	NP_001268392.1:n.1479+7G>T
NM_006306.3:c.1545+7G>T , LRG_773t2:c.1545+7G>T	NP_006297.2:n.1545+7G>T
NM_006306.4:c.1545+7G>T MANE Select	NP_006297.2:n.1545+7G>T