Canonical Allele Identifier: CA16043711
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374391
ClinVar RCV Id: RCV000415358
dbSNP Id: rs1057518670

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53415163G>C , CM000685.2:g.53415163G>C GRCh38
NC_000023.10:g.53442112G>C , CM000685.1:g.53442112G>C GRCh37
NC_000023.9:g.53458837G>C NCBI36
NG_006988.2:g.12508C>G , LRG_773:g.12508C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000322213.9:c.116C>G MANE Select ENSP00000323421.3:p.Ser39Ter
ENST00000674590.1:c.50C>G ENSP00000502626.1:p.Ser17Ter
ENST00000675065.1:n.170C>G
ENST00000675504.1:c.50C>G ENSP00000502524.1:p.Ser17Ter
ENST00000322213.8:c.116C>G ENSP00000323421.3:p.Ser39Ter
ENST00000375340.10:c.50C>G ENSP00000364489.7:p.Ser17Ter
ENST00000428014.1:c.50C>G ENSP00000413509.2:p.Ser17Ter
ENST00000463684.1:c.110-1728C>G ENSP00000476958.1:n.110-1728C>G
NM_001281463.1:c.50C>G , LRG_773t1:c.50C>G NP_001268392.1:p.Ser17Ter
NM_006306.3:c.116C>G , LRG_773t2:c.116C>G NP_006297.2:p.Ser39Ter
NM_006306.4:c.116C>G MANE Select NP_006297.2:p.Ser39Ter