Canonical Allele Identifier: CA516688549
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409487T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382566T>C , CM000685.2:g.53382566T>C GRCh38
NC_000023.10:g.53409487T>C , CM000685.1:g.53409487T>C GRCh37
NC_000023.9:g.53426212T>C NCBI36
NG_006988.2:g.45105A>G , LRG_773:g.45105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3225A>G MANE Select ENSP00000323421.3:p.Glu1075=
ENST00000674590.1:c.2457A>G ENSP00000502626.1:p.Glu819=
ENST00000675504.1:c.3159A>G ENSP00000502524.1:p.Glu1053=
ENST00000322213.8:c.3225A>G ENSP00000323421.3:p.Glu1075=
ENST00000375340.10:c.3159A>G ENSP00000364489.7:p.Glu1053=
ENST00000469129.1:n.81A>G
ENST00000470241.2:c.515A>G
NM_001281463.1:c.3159A>G , LRG_773t1:c.3159A>G NP_001268392.1:p.Glu1053=
NM_006306.3:c.3225A>G , LRG_773t2:c.3225A>G NP_006297.2:p.Glu1075=
NM_006306.4:c.3225A>G MANE Select NP_006297.2:p.Glu1075=