Canonical Allele Identifier: CA516688041
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409260G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382339G>A , CM000685.2:g.53382339G>A GRCh38
NC_000023.10:g.53409260G>A , CM000685.1:g.53409260G>A GRCh37
NC_000023.9:g.53425985G>A NCBI36
NG_006988.2:g.45332C>T , LRG_773:g.45332C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3330C>T MANE Select ENSP00000323421.3:p.Gly1110=
ENST00000674590.1:c.2562C>T ENSP00000502626.1:p.Gly854=
ENST00000675504.1:c.3264C>T ENSP00000502524.1:p.Gly1088=
ENST00000322213.8:c.3330C>T ENSP00000323421.3:p.Gly1110=
ENST00000375340.10:c.3264C>T ENSP00000364489.7:p.Gly1088=
ENST00000469129.1:n.186C>T
ENST00000470241.2:c.620C>T
NM_001281463.1:c.3264C>T , LRG_773t1:c.3264C>T NP_001268392.1:p.Gly1088=
NM_006306.3:c.3330C>T , LRG_773t2:c.3330C>T NP_006297.2:p.Gly1110=
NM_006306.4:c.3330C>T MANE Select NP_006297.2:p.Gly1110=