Canonical Allele Identifier: CA516559499
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53432581G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405649G>T , CM000685.2:g.53405649G>T GRCh38
NC_000023.10:g.53432581G>T , CM000685.1:g.53432581G>T GRCh37
NC_000023.9:g.53449306G>T NCBI36
NG_006988.2:g.22022C>A , LRG_773:g.22022C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1755C>A MANE Select ENSP00000323421.3:p.Leu585=
ENST00000674590.1:c.987C>A ENSP00000502626.1:p.Leu329=
ENST00000675065.1:n.1107C>A
ENST00000675504.1:c.1689C>A ENSP00000502524.1:p.Leu563=
ENST00000322213.8:c.1755C>A ENSP00000323421.3:p.Leu585=
ENST00000375340.10:c.1689C>A ENSP00000364489.7:p.Leu563=
NM_001281463.1:c.1689C>A , LRG_773t1:c.1689C>A NP_001268392.1:p.Leu563=
NM_006306.3:c.1755C>A , LRG_773t2:c.1755C>A NP_006297.2:p.Leu585=
NM_006306.4:c.1755C>A MANE Select NP_006297.2:p.Leu585=