Canonical Allele Identifier: CA413243449
Gene: SMC1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382332A>C , CM000685.2:g.53382332A>C GRCh38
NC_000023.10:g.53409253A>C , CM000685.1:g.53409253A>C GRCh37
NC_000023.9:g.53425978A>C NCBI36
NG_006988.2:g.45339T>G , LRG_773:g.45339T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3337T>G MANE Select ENSP00000323421.3:p.Tyr1113Asp
ENST00000674590.1:c.2569T>G ENSP00000502626.1:p.Tyr857Asp
ENST00000675504.1:c.3271T>G ENSP00000502524.1:p.Tyr1091Asp
ENST00000322213.8:c.3337T>G ENSP00000323421.3:p.Tyr1113Asp
ENST00000375340.10:c.3271T>G ENSP00000364489.7:p.Tyr1091Asp
ENST00000469129.1:n.193T>G
ENST00000470241.2:c.627T>G
NM_001281463.1:c.3271T>G , LRG_773t1:c.3271T>G NP_001268392.1:p.Tyr1091Asp
NM_006306.3:c.3337T>G , LRG_773t2:c.3337T>G NP_006297.2:p.Tyr1113Asp
NM_006306.4:c.3337T>G MANE Select NP_006297.2:p.Tyr1113Asp