Canonical Allele Identifier: CA516688289
Community Standard Title: NM_006306.4(SMC1A):c.1935A>G (p.Leu645=)
Gene: SMC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405368T>C , CM000685.2:g.53405368T>C GRCh38
NC_000023.10:g.53432300T>C , CM000685.1:g.53432300T>C GRCh37
NC_000023.9:g.53449025T>C NCBI36
NG_006988.2:g.22303A>G , LRG_773:g.22303A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006306.4:c.1935A>G MANE Select NP_006297.2:p.Leu645=
ENST00000322213.9:c.1935A>G MANE Select ENSP00000323421.3:p.Leu645=
NM_001281463.1:c.1869A>G , LRG_773t1:c.1869A>G NP_001268392.1:p.Leu623=
NM_006306.3:c.1935A>G , LRG_773t2:c.1935A>G NP_006297.2:p.Leu645=
ENST00000322213.8:c.1935A>G ENSP00000323421.3:p.Leu645=
ENST00000375340.10:c.1869A>G ENSP00000364489.7:p.Leu623=
ENST00000674590.1:c.1167A>G ENSP00000502626.1:p.Leu389=
ENST00000675065.1:n.1287A>G
ENST00000675504.1:c.1869A>G ENSP00000502524.1:p.Leu623=