Canonical Allele Identifier: CA517724483

Gene: CHM

Linked Data

• ClinVar Variation Id: 1136557
• ClinVar RCV Id: RCV001472226
• dbSNP Id: rs2147676259
• gnomAD v4: X-85963965-T-C
• MyVariant Identifiers: chrX:g.85218970T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963965T>C , CM000685.2:g.85963965T>C	GRCh38
NC_000023.10:g.85218970T>C , CM000685.1:g.85218970T>C	GRCh37
NC_000023.9:g.85105626T>C	NCBI36
NG_009874.2:g.88598A>G , LRG_699:g.88598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.402A>G MANE Select	ENSP00000350386.2:p.Ala134=
ENST00000357749.6:c.402A>G	ENSP00000350386.2:p.Ala134=
ENST00000467744.2:n.126+63526A>G
NM_000390.2:c.402A>G , LRG_699t1:c.402A>G	NP_000381.1:p.Ala134=
XM_006724615.2:c.339A>G	XP_006724678.1:p.Ala113=
XM_011530839.1:c.-43A>G	XP_011529141.1:n.-43A>G
NM_000390.3:c.402A>G	NP_000381.1:p.Ala134=
NM_001320959.1:c.-43A>G	NP_001307888.1:n.-43A>G
NM_001362517.1:c.-43A>G	NP_001349446.1:n.-43A>G
NM_001362518.1:c.-43A>G	NP_001349447.1:n.-43A>G
NM_001362519.1:c.-43A>G	NP_001349448.1:n.-43A>G
XM_017029242.2:c.402A>G	XP_016884731.1:p.Ala134=
XM_017029246.1:c.-43A>G	XP_016884735.1:n.-43A>G
XM_024452331.1:c.-43A>G	XP_024308099.1:n.-43A>G
NM_000390.4:c.402A>G MANE Select	NP_000381.1:p.Ala134=
NM_001362518.2:c.-43A>G	NP_001349447.1:n.-43A>G