Canonical Allele Identifier: CA413243811
Gene: SMC1A HGNC NCBI

Linked Data

dbSNP Id: rs1602398561

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382518A>T , CM000685.2:g.53382518A>T GRCh38
NC_000023.10:g.53409439A>T , CM000685.1:g.53409439A>T GRCh37
NC_000023.9:g.53426164A>T NCBI36
NG_006988.2:g.45153T>A , LRG_773:g.45153T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3273T>A MANE Select ENSP00000323421.3:p.Asn1091Lys
ENST00000674590.1:c.2505T>A ENSP00000502626.1:p.Asn835Lys
ENST00000675504.1:c.3207T>A ENSP00000502524.1:p.Asn1069Lys
ENST00000322213.8:c.3273T>A ENSP00000323421.3:p.Asn1091Lys
ENST00000375340.10:c.3207T>A ENSP00000364489.7:p.Asn1069Lys
ENST00000469129.1:n.129T>A
ENST00000470241.2:c.563T>A
NM_001281463.1:c.3207T>A , LRG_773t1:c.3207T>A NP_001268392.1:p.Asn1069Lys
NM_006306.3:c.3273T>A , LRG_773t2:c.3273T>A NP_006297.2:p.Asn1091Lys
NM_006306.4:c.3273T>A MANE Select NP_006297.2:p.Asn1091Lys