Canonical Allele Identifier: CA516553575
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53407607G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53380686G>T , CM000685.2:g.53380686G>T GRCh38
NC_000023.10:g.53407607G>T , CM000685.1:g.53407607G>T GRCh37
NC_000023.9:g.53424332G>T NCBI36
NG_006988.2:g.46985C>A , LRG_773:g.46985C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3552C>A MANE Select ENSP00000323421.3:p.Ala1184=
ENST00000674590.1:c.2784C>A ENSP00000502626.1:p.Ala928=
ENST00000675504.1:c.3486C>A ENSP00000502524.1:p.Ala1162=
ENST00000322213.8:c.3552C>A ENSP00000323421.3:p.Ala1184=
ENST00000375340.10:c.3486C>A ENSP00000364489.7:p.Ala1162=
ENST00000470241.2:c.772C>A
NM_001281463.1:c.3486C>A , LRG_773t1:c.3486C>A NP_001268392.1:p.Ala1162=
NM_006306.3:c.3552C>A , LRG_773t2:c.3552C>A NP_006297.2:p.Ala1184=
NM_006306.4:c.3552C>A MANE Select NP_006297.2:p.Ala1184=