Canonical Allele Identifier: CA2580101178
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1993661
ClinVar RCV Id: RCV002814651
gnomAD v4: X-53412270-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53412270G>A , CM000685.2:g.53412270G>A GRCh38
NC_000023.10:g.53439220G>A , CM000685.1:g.53439220G>A GRCh37
NC_000023.9:g.53455945G>A NCBI36
NG_006988.2:g.15401C>T , LRG_773:g.15401C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000322213.9:c.855-17C>T MANE Select ENSP00000323421.3:n.855-17C>T
ENST00000674590.1:c.346-369C>T ENSP00000502626.1:n.346-369C>T
ENST00000675065.1:n.466-369C>T
ENST00000675504.1:c.789-17C>T ENSP00000502524.1:n.789-17C>T
ENST00000322213.8:c.855-17C>T ENSP00000323421.3:n.855-17C>T
ENST00000375340.10:c.789-17C>T ENSP00000364489.7:n.789-17C>T
ENST00000463684.1:c.*388-17C>T ENSP00000476958.1:n.*388-17C>T
NM_001281463.1:c.789-17C>T , LRG_773t1:c.789-17C>T NP_001268392.1:n.789-17C>T
NM_006306.3:c.855-17C>T , LRG_773t2:c.855-17C>T NP_006297.2:n.855-17C>T
NM_006306.4:c.855-17C>T MANE Select NP_006297.2:n.855-17C>T