Canonical Allele Identifier: CA413786989

Gene: CHM

Linked Data

• MyVariant Identifiers: chrX:g.85218876C>G (hg19) ; chrX:g.85963871C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963871C>G , CM000685.2:g.85963871C>G	GRCh38
NC_000023.10:g.85218876C>G , CM000685.1:g.85218876C>G	GRCh37
NC_000023.9:g.85105532C>G	NCBI36
NG_009874.2:g.88692G>C , LRG_699:g.88692G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.496G>C MANE Select	ENSP00000350386.2:p.Ala166Pro
ENST00000357749.6:c.496G>C	ENSP00000350386.2:p.Ala166Pro
ENST00000467744.2:n.126+63620G>C
NM_000390.2:c.496G>C , LRG_699t1:c.496G>C	NP_000381.1:p.Ala166Pro
XM_006724615.2:c.433G>C	XP_006724678.1:p.Ala145Pro
XM_011530839.1:c.52G>C	XP_011529141.1:p.Ala18Pro
NM_000390.3:c.496G>C	NP_000381.1:p.Ala166Pro
NM_001320959.1:c.52G>C	NP_001307888.1:p.Ala18Pro
NM_001362517.1:c.52G>C	NP_001349446.1:p.Ala18Pro
NM_001362518.1:c.52G>C	NP_001349447.1:p.Ala18Pro
NM_001362519.1:c.52G>C	NP_001349448.1:p.Ala18Pro
XM_017029242.2:c.496G>C	XP_016884731.1:p.Ala166Pro
XM_017029246.1:c.52G>C	XP_016884735.1:p.Ala18Pro
XM_024452331.1:c.52G>C	XP_024308099.1:p.Ala18Pro
NM_000390.4:c.496G>C MANE Select	NP_000381.1:p.Ala166Pro
NM_001362518.2:c.52G>C	NP_001349447.1:p.Ala18Pro