Canonical Allele Identifier: CA413252106

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53432182G>T (hg19) ; chrX:g.53405250G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405250G>T , CM000685.2:g.53405250G>T	GRCh38
NC_000023.10:g.53432182G>T , CM000685.1:g.53432182G>T	GRCh37
NC_000023.9:g.53448907G>T	NCBI36
NG_006988.2:g.22421C>A , LRG_773:g.22421C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.2053C>A MANE Select	ENSP00000323421.3:p.Leu685Met
ENST00000674590.1:c.1285C>A	ENSP00000502626.1:p.Leu429Met
ENST00000675065.1:n.1405C>A
ENST00000675504.1:c.1987C>A	ENSP00000502524.1:p.Leu663Met
ENST00000322213.8:c.2053C>A	ENSP00000323421.3:p.Leu685Met
ENST00000375340.10:c.1987C>A	ENSP00000364489.7:p.Leu663Met
NM_001281463.1:c.1987C>A , LRG_773t1:c.1987C>A	NP_001268392.1:p.Leu663Met
NM_006306.3:c.2053C>A , LRG_773t2:c.2053C>A	NP_006297.2:p.Leu685Met
NM_006306.4:c.2053C>A MANE Select	NP_006297.2:p.Leu685Met