Canonical Allele Identifier: CA413252705

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53432435T>G (hg19) ; chrX:g.53405503T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405503T>G , CM000685.2:g.53405503T>G	GRCh38
NC_000023.10:g.53432435T>G , CM000685.1:g.53432435T>G	GRCh37
NC_000023.9:g.53449160T>G	NCBI36
NG_006988.2:g.22168A>C , LRG_773:g.22168A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1901A>C MANE Select	ENSP00000323421.3:p.Gln634Pro
ENST00000674590.1:c.1133A>C	ENSP00000502626.1:p.Gln378Pro
ENST00000675065.1:n.1253A>C
ENST00000675504.1:c.1835A>C	ENSP00000502524.1:p.Gln612Pro
ENST00000322213.8:c.1901A>C	ENSP00000323421.3:p.Gln634Pro
ENST00000375340.10:c.1835A>C	ENSP00000364489.7:p.Gln612Pro
NM_001281463.1:c.1835A>C , LRG_773t1:c.1835A>C	NP_001268392.1:p.Gln612Pro
NM_006306.3:c.1901A>C , LRG_773t2:c.1901A>C	NP_006297.2:p.Gln634Pro
NM_006306.4:c.1901A>C MANE Select	NP_006297.2:p.Gln634Pro