Canonical Allele Identifier: CA413255802

Gene: SMC1A

Linked Data

• gnomAD v4: X-53409266-C-A
• MyVariant Identifiers: chrX:g.53436197C>A (hg19) ; chrX:g.53409266C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53409266C>A , CM000685.2:g.53409266C>A	GRCh38
NC_000023.10:g.53436197C>A , CM000685.1:g.53436197C>A	GRCh37
NC_000023.9:g.53452922C>A	NCBI36
NG_006988.2:g.18405G>T , LRG_773:g.18405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1341G>T MANE Select	ENSP00000323421.3:p.Gln447His
ENST00000674590.1:c.573G>T	ENSP00000502626.1:p.Gln191His
ENST00000675065.1:n.693G>T
ENST00000675504.1:c.1275G>T	ENSP00000502524.1:p.Gln425His
ENST00000322213.8:c.1341G>T	ENSP00000323421.3:p.Gln447His
ENST00000375340.10:c.1275G>T	ENSP00000364489.7:p.Gln425His
NM_001281463.1:c.1275G>T , LRG_773t1:c.1275G>T	NP_001268392.1:p.Gln425His
NM_006306.3:c.1341G>T , LRG_773t2:c.1341G>T	NP_006297.2:p.Gln447His
NM_006306.4:c.1341G>T MANE Select	NP_006297.2:p.Gln447His