Canonical Allele Identifier: CA517491204

Gene: CHM

Linked Data

• gnomAD v4: X-85958881-G-T
• MyVariant Identifiers: chrX:g.85213886G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85958881G>T , CM000685.2:g.85958881G>T	GRCh38
NC_000023.10:g.85213886G>T , CM000685.1:g.85213886G>T	GRCh37
NC_000023.9:g.85100542G>T	NCBI36
NG_009874.2:g.93682C>A , LRG_699:g.93682C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.799C>A MANE Select	ENSP00000350386.2:p.Arg267=
ENST00000357749.6:c.799C>A	ENSP00000350386.2:p.Arg267=
ENST00000467744.2:n.126+68610C>A
NM_000390.2:c.799C>A , LRG_699t1:c.799C>A	NP_000381.1:p.Arg267=
XM_006724615.2:c.736C>A	XP_006724678.1:p.Arg246=
XM_011530839.1:c.355C>A	XP_011529141.1:p.Arg119=
NM_000390.3:c.799C>A	NP_000381.1:p.Arg267=
NM_001320959.1:c.355C>A	NP_001307888.1:p.Arg119=
NM_001362517.1:c.355C>A	NP_001349446.1:p.Arg119=
NM_001362518.1:c.355C>A	NP_001349447.1:p.Arg119=
NM_001362519.1:c.355C>A	NP_001349448.1:p.Arg119=
XM_017029242.2:c.799C>A	XP_016884731.1:p.Arg267=
XM_017029246.1:c.355C>A	XP_016884735.1:p.Arg119=
XM_024452331.1:c.355C>A	XP_024308099.1:p.Arg119=
NM_000390.4:c.799C>A MANE Select	NP_000381.1:p.Arg267=
NM_001362518.2:c.355C>A	NP_001349447.1:p.Arg119=