Canonical Allele Identifier: CA516688204

Gene: SMC1A

Linked Data

• ClinVar Variation Id: 1566512
• ClinVar RCV Id: RCV002207449
• dbSNP Id: rs2146599598
• MyVariant Identifiers: chrX:g.53432258C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405326C>T , CM000685.2:g.53405326C>T	GRCh38
NC_000023.10:g.53432258C>T , CM000685.1:g.53432258C>T	GRCh37
NC_000023.9:g.53448983C>T	NCBI36
NG_006988.2:g.22345G>A , LRG_773:g.22345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1977G>A MANE Select	ENSP00000323421.3:p.Leu659=
ENST00000674590.1:c.1209G>A	ENSP00000502626.1:p.Leu403=
ENST00000675065.1:n.1329G>A
ENST00000675504.1:c.1911G>A	ENSP00000502524.1:p.Leu637=
ENST00000322213.8:c.1977G>A	ENSP00000323421.3:p.Leu659=
ENST00000375340.10:c.1911G>A	ENSP00000364489.7:p.Leu637=
NM_001281463.1:c.1911G>A , LRG_773t1:c.1911G>A	NP_001268392.1:p.Leu637=
NM_006306.3:c.1977G>A , LRG_773t2:c.1977G>A	NP_006297.2:p.Leu659=
NM_006306.4:c.1977G>A MANE Select	NP_006297.2:p.Leu659=