Canonical Allele Identifier: CA10465528

Gene: CHM

Linked Data

• dbSNP Id: rs367902196
• ExAC: X:85213885 C / T
• gnomAD v2: X-85213885-C-T
• gnomAD v4: X-85958880-C-T
• MyVariant Identifiers: chrX:g.85213885C>T (hg19) ; chrX:g.85958880C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85958880C>T , CM000685.2:g.85958880C>T	GRCh38
NC_000023.10:g.85213885C>T , CM000685.1:g.85213885C>T	GRCh37
NC_000023.9:g.85100541C>T	NCBI36
NG_009874.2:g.93683G>A , LRG_699:g.93683G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.800G>A MANE Select	ENSP00000350386.2:p.Arg267Gln
ENST00000357749.6:c.800G>A	ENSP00000350386.2:p.Arg267Gln
ENST00000467744.2:n.126+68611G>A
NM_000390.2:c.800G>A , LRG_699t1:c.800G>A	NP_000381.1:p.Arg267Gln
XM_006724615.2:c.737G>A	XP_006724678.1:p.Arg246Gln
XM_011530839.1:c.356G>A	XP_011529141.1:p.Arg119Gln
NM_000390.3:c.800G>A	NP_000381.1:p.Arg267Gln
NM_001320959.1:c.356G>A	NP_001307888.1:p.Arg119Gln
NM_001362517.1:c.356G>A	NP_001349446.1:p.Arg119Gln
NM_001362518.1:c.356G>A	NP_001349447.1:p.Arg119Gln
NM_001362519.1:c.356G>A	NP_001349448.1:p.Arg119Gln
XM_017029242.2:c.800G>A	XP_016884731.1:p.Arg267Gln
XM_017029246.1:c.356G>A	XP_016884735.1:p.Arg119Gln
XM_024452331.1:c.356G>A	XP_024308099.1:p.Arg119Gln
NM_000390.4:c.800G>A MANE Select	NP_000381.1:p.Arg267Gln
NM_001362518.2:c.356G>A	NP_001349447.1:p.Arg119Gln