Canonical Allele Identifier: CA413252844

Gene: SMC1A

Linked Data

• COSMIC: COSM6031470
• MyVariant Identifiers: chrX:g.53432472C>T (hg19) ; chrX:g.53405540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405540C>T , CM000685.2:g.53405540C>T	GRCh38
NC_000023.10:g.53432472C>T , CM000685.1:g.53432472C>T	GRCh37
NC_000023.9:g.53449197C>T	NCBI36
NG_006988.2:g.22131G>A , LRG_773:g.22131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1864G>A MANE Select	ENSP00000323421.3:p.Val622Met
ENST00000674590.1:c.1096G>A	ENSP00000502626.1:p.Val366Met
ENST00000675065.1:n.1216G>A
ENST00000675504.1:c.1798G>A	ENSP00000502524.1:p.Val600Met
ENST00000322213.8:c.1864G>A	ENSP00000323421.3:p.Val622Met
ENST00000375340.10:c.1798G>A	ENSP00000364489.7:p.Val600Met
NM_001281463.1:c.1798G>A , LRG_773t1:c.1798G>A	NP_001268392.1:p.Val600Met
NM_006306.3:c.1864G>A , LRG_773t2:c.1864G>A	NP_006297.2:p.Val622Met
NM_006306.4:c.1864G>A MANE Select	NP_006297.2:p.Val622Met