Canonical Allele Identifier: CA516688702
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53439116T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53412166T>G , CM000685.2:g.53412166T>G GRCh38
NC_000023.10:g.53439116T>G , CM000685.1:g.53439116T>G GRCh37
NC_000023.9:g.53455841T>G NCBI36
NG_006988.2:g.15505A>C , LRG_773:g.15505A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.942A>C MANE Select ENSP00000323421.3:p.Ala314=
ENST00000674590.1:c.346-265A>C ENSP00000502626.1:n.346-265A>C
ENST00000675065.1:n.466-265A>C
ENST00000675504.1:c.876A>C ENSP00000502524.1:p.Ala292=
ENST00000322213.8:c.942A>C ENSP00000323421.3:p.Ala314=
ENST00000375340.10:c.876A>C ENSP00000364489.7:p.Ala292=
ENST00000463684.1:c.*475A>C ENSP00000476958.1:n.*475A>C
NM_001281463.1:c.876A>C , LRG_773t1:c.876A>C NP_001268392.1:p.Ala292=
NM_006306.3:c.942A>C , LRG_773t2:c.942A>C NP_006297.2:p.Ala314=
NM_006306.4:c.942A>C MANE Select NP_006297.2:p.Ala314=