Canonical Allele Identifier: CA516688706
Gene: SMC1A HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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