Canonical Allele Identifier: CA413252685

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53432430G>C (hg19) ; chrX:g.53405498G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405498G>C , CM000685.2:g.53405498G>C	GRCh38
NC_000023.10:g.53432430G>C , CM000685.1:g.53432430G>C	GRCh37
NC_000023.9:g.53449155G>C	NCBI36
NG_006988.2:g.22173C>G , LRG_773:g.22173C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1906C>G MANE Select	ENSP00000323421.3:p.His636Asp
ENST00000674590.1:c.1138C>G	ENSP00000502626.1:p.His380Asp
ENST00000675065.1:n.1258C>G
ENST00000675504.1:c.1840C>G	ENSP00000502524.1:p.His614Asp
ENST00000322213.8:c.1906C>G	ENSP00000323421.3:p.His636Asp
ENST00000375340.10:c.1840C>G	ENSP00000364489.7:p.His614Asp
NM_001281463.1:c.1840C>G , LRG_773t1:c.1840C>G	NP_001268392.1:p.His614Asp
NM_006306.3:c.1906C>G , LRG_773t2:c.1906C>G	NP_006297.2:p.His636Asp
NM_006306.4:c.1906C>G MANE Select	NP_006297.2:p.His636Asp