Canonical Allele Identifier: CA413243218

Gene: SMC1A

Linked Data

• COSMIC: COSM5956930
• MyVariant Identifiers: chrX:g.53409151A>G (hg19) ; chrX:g.53382230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382230A>G , CM000685.2:g.53382230A>G	GRCh38
NC_000023.10:g.53409151A>G , CM000685.1:g.53409151A>G	GRCh37
NC_000023.9:g.53425876A>G	NCBI36
NG_006988.2:g.45441T>C , LRG_773:g.45441T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.3437+2T>C MANE Select	ENSP00000323421.3:n.3437+2T>C
ENST00000674590.1:c.2669+2T>C	ENSP00000502626.1:n.2669+2T>C
ENST00000675504.1:c.3371+2T>C	ENSP00000502524.1:n.3371+2T>C
ENST00000322213.8:c.3437+2T>C	ENSP00000323421.3:n.3437+2T>C
ENST00000375340.10:c.3371+2T>C	ENSP00000364489.7:n.3371+2T>C
ENST00000469129.1:n.295T>C
ENST00000470241.2:c.727+2T>C
NM_001281463.1:c.3371+2T>C , LRG_773t1:c.3371+2T>C	NP_001268392.1:n.3371+2T>C
NM_006306.3:c.3437+2T>C , LRG_773t2:c.3437+2T>C	NP_006297.2:n.3437+2T>C
NM_006306.4:c.3437+2T>C MANE Select	NP_006297.2:n.3437+2T>C