Canonical Allele Identifier: CA516688012
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409221C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382300C>A , CM000685.2:g.53382300C>A GRCh38
NC_000023.10:g.53409221C>A , CM000685.1:g.53409221C>A GRCh37
NC_000023.9:g.53425946C>A NCBI36
NG_006988.2:g.45371G>T , LRG_773:g.45371G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000322213.9:c.3369G>T MANE Select ENSP00000323421.3:p.Arg1123=
ENST00000674590.1:c.2601G>T ENSP00000502626.1:p.Arg867=
ENST00000675504.1:c.3303G>T ENSP00000502524.1:p.Arg1101=
ENST00000322213.8:c.3369G>T ENSP00000323421.3:p.Arg1123=
ENST00000375340.10:c.3303G>T ENSP00000364489.7:p.Arg1101=
ENST00000469129.1:n.225G>T
ENST00000470241.2:c.659G>T
NM_001281463.1:c.3303G>T , LRG_773t1:c.3303G>T NP_001268392.1:p.Arg1101=
NM_006306.3:c.3369G>T , LRG_773t2:c.3369G>T NP_006297.2:p.Arg1123=
NM_006306.4:c.3369G>T MANE Select NP_006297.2:p.Arg1123=