Canonical Allele Identifier: CA516688302

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53432306T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405374T>C , CM000685.2:g.53405374T>C	GRCh38
NC_000023.10:g.53432306T>C , CM000685.1:g.53432306T>C	GRCh37
NC_000023.9:g.53449031T>C	NCBI36
NG_006988.2:g.22297A>G , LRG_773:g.22297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1929A>G MANE Select	ENSP00000323421.3:p.Gly643=
ENST00000674590.1:c.1161A>G	ENSP00000502626.1:p.Gly387=
ENST00000675065.1:n.1281A>G
ENST00000675504.1:c.1863A>G	ENSP00000502524.1:p.Gly621=
ENST00000322213.8:c.1929A>G	ENSP00000323421.3:p.Gly643=
ENST00000375340.10:c.1863A>G	ENSP00000364489.7:p.Gly621=
NM_001281463.1:c.1863A>G , LRG_773t1:c.1863A>G	NP_001268392.1:p.Gly621=
NM_006306.3:c.1929A>G , LRG_773t2:c.1929A>G	NP_006297.2:p.Gly643=
NM_006306.4:c.1929A>G MANE Select	NP_006297.2:p.Gly643=