Canonical Allele Identifier: CA516561964

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53436158T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53409227T>C , CM000685.2:g.53409227T>C	GRCh38
NC_000023.10:g.53436158T>C , CM000685.1:g.53436158T>C	GRCh37
NC_000023.9:g.53452883T>C	NCBI36
NG_006988.2:g.18444A>G , LRG_773:g.18444A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1380A>G MANE Select	ENSP00000323421.3:p.Thr460=
ENST00000674590.1:c.612A>G	ENSP00000502626.1:p.Thr204=
ENST00000675065.1:n.732A>G
ENST00000675504.1:c.1314A>G	ENSP00000502524.1:p.Thr438=
ENST00000322213.8:c.1380A>G	ENSP00000323421.3:p.Thr460=
ENST00000375340.10:c.1314A>G	ENSP00000364489.7:p.Thr438=
NM_001281463.1:c.1314A>G , LRG_773t1:c.1314A>G	NP_001268392.1:p.Thr438=
NM_006306.3:c.1380A>G , LRG_773t2:c.1380A>G	NP_006297.2:p.Thr460=
NM_006306.4:c.1380A>G MANE Select	NP_006297.2:p.Thr460=