Canonical Allele Identifier: CA516688193
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53432512G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405580G>C , CM000685.2:g.53405580G>C GRCh38
NC_000023.10:g.53432512G>C , CM000685.1:g.53432512G>C GRCh37
NC_000023.9:g.53449237G>C NCBI36
NG_006988.2:g.22091C>G , LRG_773:g.22091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1824C>G MANE Select ENSP00000323421.3:p.Ala608=
ENST00000674590.1:c.1056C>G ENSP00000502626.1:p.Ala352=
ENST00000675065.1:n.1176C>G
ENST00000675504.1:c.1758C>G ENSP00000502524.1:p.Ala586=
ENST00000322213.8:c.1824C>G ENSP00000323421.3:p.Ala608=
ENST00000375340.10:c.1758C>G ENSP00000364489.7:p.Ala586=
NM_001281463.1:c.1758C>G , LRG_773t1:c.1758C>G NP_001268392.1:p.Ala586=
NM_006306.3:c.1824C>G , LRG_773t2:c.1824C>G NP_006297.2:p.Ala608=
NM_006306.4:c.1824C>G MANE Select NP_006297.2:p.Ala608=