Canonical Allele Identifier: CA413243649

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53409295C>A (hg19) ; chrX:g.53382374C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382374C>A , CM000685.2:g.53382374C>A	GRCh38
NC_000023.10:g.53409295C>A , CM000685.1:g.53409295C>A	GRCh37
NC_000023.9:g.53426020C>A	NCBI36
NG_006988.2:g.45297G>T , LRG_773:g.45297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.3295G>T MANE Select	ENSP00000323421.3:p.Gly1099Cys
ENST00000674590.1:c.2527G>T	ENSP00000502626.1:p.Gly843Cys
ENST00000675504.1:c.3229G>T	ENSP00000502524.1:p.Gly1077Cys
ENST00000322213.8:c.3295G>T	ENSP00000323421.3:p.Gly1099Cys
ENST00000375340.10:c.3229G>T	ENSP00000364489.7:p.Gly1077Cys
ENST00000469129.1:n.151G>T
ENST00000470241.2:c.585G>T
NM_001281463.1:c.3229G>T , LRG_773t1:c.3229G>T	NP_001268392.1:p.Gly1077Cys
NM_006306.3:c.3295G>T , LRG_773t2:c.3295G>T	NP_006297.2:p.Gly1099Cys
NM_006306.4:c.3295G>T MANE Select	NP_006297.2:p.Gly1099Cys