Canonical Allele Identifier: CA516688214
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53432264A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405332A>G , CM000685.2:g.53405332A>G GRCh38
NC_000023.10:g.53432264A>G , CM000685.1:g.53432264A>G GRCh37
NC_000023.9:g.53448989A>G NCBI36
NG_006988.2:g.22339T>C , LRG_773:g.22339T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1971T>C MANE Select ENSP00000323421.3:p.Ser657=
ENST00000674590.1:c.1203T>C ENSP00000502626.1:p.Ser401=
ENST00000675065.1:n.1323T>C
ENST00000675504.1:c.1905T>C ENSP00000502524.1:p.Ser635=
ENST00000322213.8:c.1971T>C ENSP00000323421.3:p.Ser657=
ENST00000375340.10:c.1905T>C ENSP00000364489.7:p.Ser635=
NM_001281463.1:c.1905T>C , LRG_773t1:c.1905T>C NP_001268392.1:p.Ser635=
NM_006306.3:c.1971T>C , LRG_773t2:c.1971T>C NP_006297.2:p.Ser657=
NM_006306.4:c.1971T>C MANE Select NP_006297.2:p.Ser657=