Canonical Allele Identifier: CA516688019

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53409227G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382306G>T , CM000685.2:g.53382306G>T	GRCh38
NC_000023.10:g.53409227G>T , CM000685.1:g.53409227G>T	GRCh37
NC_000023.9:g.53425952G>T	NCBI36
NG_006988.2:g.45365C>A , LRG_773:g.45365C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000322213.9:c.3363C>A MANE Select	ENSP00000323421.3:p.Arg1121=
ENST00000674590.1:c.2595C>A	ENSP00000502626.1:p.Arg865=
ENST00000675504.1:c.3297C>A	ENSP00000502524.1:p.Arg1099=
ENST00000322213.8:c.3363C>A	ENSP00000323421.3:p.Arg1121=
ENST00000375340.10:c.3297C>A	ENSP00000364489.7:p.Arg1099=
ENST00000469129.1:n.219C>A
ENST00000470241.2:c.653C>A
NM_001281463.1:c.3297C>A , LRG_773t1:c.3297C>A	NP_001268392.1:p.Arg1099=
NM_006306.3:c.3363C>A , LRG_773t2:c.3363C>A	NP_006297.2:p.Arg1121=
NM_006306.4:c.3363C>A MANE Select	NP_006297.2:p.Arg1121=