Canonical Allele Identifier: CA876290489

Gene: SMC1A

Linked Data

• dbSNP Id: rs1347501225
• MyVariant Identifiers: chrX:g.53414668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53414668G>A , CM000685.2:g.53414668G>A	GRCh38
NC_000023.10:g.53441617G>A , CM000685.1:g.53441617G>A	GRCh37
NC_000023.9:g.53458342G>A	NCBI36
NG_006988.2:g.13003C>T , LRG_773:g.13003C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322213.9:c.411+90C>T MANE Select	ENSP00000323421.3:n.411+90C>T
ENST00000674590.1:c.345+90C>T	ENSP00000502626.1:n.345+90C>T
ENST00000675065.1:n.465+90C>T
ENST00000675504.1:c.345+90C>T	ENSP00000502524.1:n.345+90C>T
ENST00000322213.8:c.411+90C>T	ENSP00000323421.3:n.411+90C>T
ENST00000375340.10:c.345+90C>T	ENSP00000364489.7:n.345+90C>T
ENST00000428014.1:c.345+90C>T	ENSP00000413509.2:n.345+90C>T
ENST00000463684.1:c.110-1233C>T	ENSP00000476958.1:n.110-1233C>T
NM_001281463.1:c.345+90C>T , LRG_773t1:c.345+90C>T	NP_001268392.1:n.345+90C>T
NM_006306.3:c.411+90C>T , LRG_773t2:c.411+90C>T	NP_006297.2:n.411+90C>T
NM_006306.4:c.411+90C>T MANE Select	NP_006297.2:n.411+90C>T