Canonical Allele Identifier: CA516553406
Gene: SMC1A HGNC NCBI

Linked Data

dbSNP Id: rs2075578765
MyVariant Identifiers: chrX:g.53407562G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53380641G>A , CM000685.2:g.53380641G>A GRCh38
NC_000023.10:g.53407562G>A , CM000685.1:g.53407562G>A GRCh37
NC_000023.9:g.53424287G>A NCBI36
NG_006988.2:g.47030C>T , LRG_773:g.47030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3597C>T MANE Select ENSP00000323421.3:p.Ser1199=
ENST00000674590.1:c.2829C>T ENSP00000502626.1:p.Ser943=
ENST00000675504.1:c.3531C>T ENSP00000502524.1:p.Ser1177=
ENST00000322213.8:c.3597C>T ENSP00000323421.3:p.Ser1199=
ENST00000375340.10:c.3531C>T ENSP00000364489.7:p.Ser1177=
ENST00000470241.2:c.817C>T
NM_001281463.1:c.3531C>T , LRG_773t1:c.3531C>T NP_001268392.1:p.Ser1177=
NM_006306.3:c.3597C>T , LRG_773t2:c.3597C>T NP_006297.2:p.Ser1199=
NM_006306.4:c.3597C>T MANE Select NP_006297.2:p.Ser1199=