Canonical Allele Identifier: CA516688288
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53432300T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405368T>A , CM000685.2:g.53405368T>A GRCh38
NC_000023.10:g.53432300T>A , CM000685.1:g.53432300T>A GRCh37
NC_000023.9:g.53449025T>A NCBI36
NG_006988.2:g.22303A>T , LRG_773:g.22303A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1935A>T MANE Select ENSP00000323421.3:p.Leu645=
ENST00000674590.1:c.1167A>T ENSP00000502626.1:p.Leu389=
ENST00000675065.1:n.1287A>T
ENST00000675504.1:c.1869A>T ENSP00000502524.1:p.Leu623=
ENST00000322213.8:c.1935A>T ENSP00000323421.3:p.Leu645=
ENST00000375340.10:c.1869A>T ENSP00000364489.7:p.Leu623=
NM_001281463.1:c.1869A>T , LRG_773t1:c.1869A>T NP_001268392.1:p.Leu623=
NM_006306.3:c.1935A>T , LRG_773t2:c.1935A>T NP_006297.2:p.Leu645=
NM_006306.4:c.1935A>T MANE Select NP_006297.2:p.Leu645=