Canonical Allele Identifier: CA516688520
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53409442G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382521G>C , CM000685.2:g.53382521G>C GRCh38
NC_000023.10:g.53409442G>C , CM000685.1:g.53409442G>C GRCh37
NC_000023.9:g.53426167G>C NCBI36
NG_006988.2:g.45150C>G , LRG_773:g.45150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3270C>G MANE Select ENSP00000323421.3:p.Arg1090=
ENST00000674590.1:c.2502C>G ENSP00000502626.1:p.Arg834=
ENST00000675504.1:c.3204C>G ENSP00000502524.1:p.Arg1068=
ENST00000322213.8:c.3270C>G ENSP00000323421.3:p.Arg1090=
ENST00000375340.10:c.3204C>G ENSP00000364489.7:p.Arg1068=
ENST00000469129.1:n.126C>G
ENST00000470241.2:c.560C>G
NM_001281463.1:c.3204C>G , LRG_773t1:c.3204C>G NP_001268392.1:p.Arg1068=
NM_006306.3:c.3270C>G , LRG_773t2:c.3270C>G NP_006297.2:p.Arg1090=
NM_006306.4:c.3270C>G MANE Select NP_006297.2:p.Arg1090=