Canonical Allele Identifier: CA516688707
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53439122C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53412172C>T , CM000685.2:g.53412172C>T GRCh38
NC_000023.10:g.53439122C>T , CM000685.1:g.53439122C>T GRCh37
NC_000023.9:g.53455847C>T NCBI36
NG_006988.2:g.15499G>A , LRG_773:g.15499G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.936G>A MANE Select ENSP00000323421.3:p.Leu312=
ENST00000674590.1:c.346-271G>A ENSP00000502626.1:n.346-271G>A
ENST00000675065.1:n.466-271G>A
ENST00000675504.1:c.870G>A ENSP00000502524.1:p.Leu290=
ENST00000322213.8:c.936G>A ENSP00000323421.3:p.Leu312=
ENST00000375340.10:c.870G>A ENSP00000364489.7:p.Leu290=
ENST00000463684.1:c.*469G>A ENSP00000476958.1:n.*469G>A
NM_001281463.1:c.870G>A , LRG_773t1:c.870G>A NP_001268392.1:p.Leu290=
NM_006306.3:c.936G>A , LRG_773t2:c.936G>A NP_006297.2:p.Leu312=
NM_006306.4:c.936G>A MANE Select NP_006297.2:p.Leu312=