Canonical Allele Identifier: CA516688279
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53432551A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405619A>T , CM000685.2:g.53405619A>T GRCh38
NC_000023.10:g.53432551A>T , CM000685.1:g.53432551A>T GRCh37
NC_000023.9:g.53449276A>T NCBI36
NG_006988.2:g.22052T>A , LRG_773:g.22052T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1785T>A MANE Select ENSP00000323421.3:p.Ile595=
ENST00000674590.1:c.1017T>A ENSP00000502626.1:p.Ile339=
ENST00000675065.1:n.1137T>A
ENST00000675504.1:c.1719T>A ENSP00000502524.1:p.Ile573=
ENST00000322213.8:c.1785T>A ENSP00000323421.3:p.Ile595=
ENST00000375340.10:c.1719T>A ENSP00000364489.7:p.Ile573=
NM_001281463.1:c.1719T>A , LRG_773t1:c.1719T>A NP_001268392.1:p.Ile573=
NM_006306.3:c.1785T>A , LRG_773t2:c.1785T>A NP_006297.2:p.Ile595=
NM_006306.4:c.1785T>A MANE Select NP_006297.2:p.Ile595=