Canonical Allele Identifier: CA516688530
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409454C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382533C>T , CM000685.2:g.53382533C>T GRCh38
NC_000023.10:g.53409454C>T , CM000685.1:g.53409454C>T GRCh37
NC_000023.9:g.53426179C>T NCBI36
NG_006988.2:g.45138G>A , LRG_773:g.45138G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3258G>A MANE Select ENSP00000323421.3:p.Lys1086=
ENST00000674590.1:c.2490G>A ENSP00000502626.1:p.Lys830=
ENST00000675504.1:c.3192G>A ENSP00000502524.1:p.Lys1064=
ENST00000322213.8:c.3258G>A ENSP00000323421.3:p.Lys1086=
ENST00000375340.10:c.3192G>A ENSP00000364489.7:p.Lys1064=
ENST00000469129.1:n.114G>A
ENST00000470241.2:c.548G>A
NM_001281463.1:c.3192G>A , LRG_773t1:c.3192G>A NP_001268392.1:p.Lys1064=
NM_006306.3:c.3258G>A , LRG_773t2:c.3258G>A NP_006297.2:p.Lys1086=
NM_006306.4:c.3258G>A MANE Select NP_006297.2:p.Lys1086=