Canonical Allele Identifier: CA413786697

Gene: CHM

Linked Data

• MyVariant Identifiers: chrX:g.85218794G>A (hg19) ; chrX:g.85963789G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963789G>A , CM000685.2:g.85963789G>A	GRCh38
NC_000023.10:g.85218794G>A , CM000685.1:g.85218794G>A	GRCh37
NC_000023.9:g.85105450G>A	NCBI36
NG_009874.2:g.88774C>T , LRG_699:g.88774C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.578C>T MANE Select	ENSP00000350386.2:p.Ala193Val
ENST00000357749.6:c.578C>T	ENSP00000350386.2:p.Ala193Val
ENST00000467744.2:n.126+63702C>T
NM_000390.2:c.578C>T , LRG_699t1:c.578C>T	NP_000381.1:p.Ala193Val
XM_006724615.2:c.515C>T	XP_006724678.1:p.Ala172Val
XM_011530839.1:c.134C>T	XP_011529141.1:p.Ala45Val
NM_000390.3:c.578C>T	NP_000381.1:p.Ala193Val
NM_001320959.1:c.134C>T	NP_001307888.1:p.Ala45Val
NM_001362517.1:c.134C>T	NP_001349446.1:p.Ala45Val
NM_001362518.1:c.134C>T	NP_001349447.1:p.Ala45Val
NM_001362519.1:c.134C>T	NP_001349448.1:p.Ala45Val
XM_017029242.2:c.578C>T	XP_016884731.1:p.Ala193Val
XM_017029246.1:c.134C>T	XP_016884735.1:p.Ala45Val
XM_024452331.1:c.134C>T	XP_024308099.1:p.Ala45Val
NM_000390.4:c.578C>T MANE Select	NP_000381.1:p.Ala193Val
NM_001362518.2:c.134C>T	NP_001349447.1:p.Ala45Val