Canonical Allele Identifier: CA413243832

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53409441T>C (hg19) ; chrX:g.53382520T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382520T>C , CM000685.2:g.53382520T>C	GRCh38
NC_000023.10:g.53409441T>C , CM000685.1:g.53409441T>C	GRCh37
NC_000023.9:g.53426166T>C	NCBI36
NG_006988.2:g.45151A>G , LRG_773:g.45151A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.3271A>G MANE Select	ENSP00000323421.3:p.Asn1091Asp
ENST00000674590.1:c.2503A>G	ENSP00000502626.1:p.Asn835Asp
ENST00000675504.1:c.3205A>G	ENSP00000502524.1:p.Asn1069Asp
ENST00000322213.8:c.3271A>G	ENSP00000323421.3:p.Asn1091Asp
ENST00000375340.10:c.3205A>G	ENSP00000364489.7:p.Asn1069Asp
ENST00000469129.1:n.127A>G
ENST00000470241.2:c.561A>G
NM_001281463.1:c.3205A>G , LRG_773t1:c.3205A>G	NP_001268392.1:p.Asn1069Asp
NM_006306.3:c.3271A>G , LRG_773t2:c.3271A>G	NP_006297.2:p.Asn1091Asp
NM_006306.4:c.3271A>G MANE Select	NP_006297.2:p.Asn1091Asp