Canonical Allele Identifier: CA1133167748

Gene: SMC1A

Linked Data

• dbSNP Id: rs782501516
• gnomAD v3: X-53382198-C-T
• gnomAD v4: X-53382198-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382198C>T , CM000685.2:g.53382198C>T	GRCh38
NC_000023.10:g.53409119C>T , CM000685.1:g.53409119C>T	GRCh37
NC_000023.9:g.53425844C>T	NCBI36
NG_006988.2:g.45473G>A , LRG_773:g.45473G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.3437+34G>A MANE Select	ENSP00000323421.3:n.3437+34G>A
ENST00000674590.1:c.2669+34G>A	ENSP00000502626.1:n.2669+34G>A
ENST00000675504.1:c.3371+34G>A	ENSP00000502524.1:n.3371+34G>A
ENST00000322213.8:c.3437+34G>A	ENSP00000323421.3:n.3437+34G>A
ENST00000375340.10:c.3371+34G>A	ENSP00000364489.7:n.3371+34G>A
ENST00000469129.1:n.327G>A
ENST00000470241.2:c.727+34G>A
NM_001281463.1:c.3371+34G>A , LRG_773t1:c.3371+34G>A	NP_001268392.1:n.3371+34G>A
NM_006306.3:c.3437+34G>A , LRG_773t2:c.3437+34G>A	NP_006297.2:n.3437+34G>A
NM_006306.4:c.3437+34G>A MANE Select	NP_006297.2:n.3437+34G>A