Canonical Allele Identifier: CA517491199
Gene: CHM HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.85213878T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85958873T>G , CM000685.2:g.85958873T>G GRCh38
NC_000023.10:g.85213878T>G , CM000685.1:g.85213878T>G GRCh37
NC_000023.9:g.85100534T>G NCBI36
NG_009874.2:g.93690A>C , LRG_699:g.93690A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.807A>C MANE Select ENSP00000350386.2:p.Gly269=
ENST00000357749.6:c.807A>C ENSP00000350386.2:p.Gly269=
ENST00000467744.2:n.126+68618A>C
NM_000390.2:c.807A>C , LRG_699t1:c.807A>C NP_000381.1:p.Gly269=
XM_006724615.2:c.744A>C XP_006724678.1:p.Gly248=
XM_011530839.1:c.363A>C XP_011529141.1:p.Gly121=
NM_000390.3:c.807A>C NP_000381.1:p.Gly269=
NM_001320959.1:c.363A>C NP_001307888.1:p.Gly121=
NM_001362517.1:c.363A>C NP_001349446.1:p.Gly121=
NM_001362518.1:c.363A>C NP_001349447.1:p.Gly121=
NM_001362519.1:c.363A>C NP_001349448.1:p.Gly121=
XM_017029242.2:c.807A>C XP_016884731.1:p.Gly269=
XM_017029246.1:c.363A>C XP_016884735.1:p.Gly121=
XM_024452331.1:c.363A>C XP_024308099.1:p.Gly121=
NM_000390.4:c.807A>C MANE Select NP_000381.1:p.Gly269=
NM_001362518.2:c.363A>C NP_001349447.1:p.Gly121=