Canonical Allele Identifier: CA516688494
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409281A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382360A>T , CM000685.2:g.53382360A>T GRCh38
NC_000023.10:g.53409281A>T , CM000685.1:g.53409281A>T GRCh37
NC_000023.9:g.53426006A>T NCBI36
NG_006988.2:g.45311T>A , LRG_773:g.45311T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3309T>A MANE Select ENSP00000323421.3:p.Pro1103=
ENST00000674590.1:c.2541T>A ENSP00000502626.1:p.Pro847=
ENST00000675504.1:c.3243T>A ENSP00000502524.1:p.Pro1081=
ENST00000322213.8:c.3309T>A ENSP00000323421.3:p.Pro1103=
ENST00000375340.10:c.3243T>A ENSP00000364489.7:p.Pro1081=
ENST00000469129.1:n.165T>A
ENST00000470241.2:c.599T>A
NM_001281463.1:c.3243T>A , LRG_773t1:c.3243T>A NP_001268392.1:p.Pro1081=
NM_006306.3:c.3309T>A , LRG_773t2:c.3309T>A NP_006297.2:p.Pro1103=
NM_006306.4:c.3309T>A MANE Select NP_006297.2:p.Pro1103=