Canonical Allele Identifier: CA516561429
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53436029T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53409098T>A , CM000685.2:g.53409098T>A GRCh38
NC_000023.10:g.53436029T>A , CM000685.1:g.53436029T>A GRCh37
NC_000023.9:g.53452754T>A NCBI36
NG_006988.2:g.18573A>T , LRG_773:g.18573A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1509A>T MANE Select ENSP00000323421.3:p.Ile503=
ENST00000674590.1:c.741A>T ENSP00000502626.1:p.Ile247=
ENST00000675065.1:n.861A>T
ENST00000675504.1:c.1443A>T ENSP00000502524.1:p.Ile481=
ENST00000322213.8:c.1509A>T ENSP00000323421.3:p.Ile503=
ENST00000375340.10:c.1443A>T ENSP00000364489.7:p.Ile481=
NM_001281463.1:c.1443A>T , LRG_773t1:c.1443A>T NP_001268392.1:p.Ile481=
NM_006306.3:c.1509A>T , LRG_773t2:c.1509A>T NP_006297.2:p.Ile503=
NM_006306.4:c.1509A>T MANE Select NP_006297.2:p.Ile503=