Canonical Allele Identifier: CA645509232

Gene: CHM

Linked Data

• ClinVar Variation Id: 438064
• ClinVar RCV Id: RCV000504724 ; RCV000504914 ; RCV001542630
• dbSNP Id: rs1555955061
• MyVariant Identifiers: chrX:g.85220593T>C (hg19) ; chrX:g.85965588T>C (hg38)
• PubMed: PMID:28041643

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85965588T>C , CM000685.2:g.85965588T>C	GRCh38
NC_000023.10:g.85220593T>C , CM000685.1:g.85220593T>C	GRCh37
NC_000023.9:g.85107249T>C	NCBI36
NG_009874.2:g.86975A>G , LRG_699:g.86975A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.315-1536A>G MANE Select	ENSP00000350386.2:n.315-1536A>G
ENST00000357749.6:c.315-1536A>G	ENSP00000350386.2:n.315-1536A>G
ENST00000467744.2:n.126+61903A>G
NM_000390.2:c.315-1536A>G , LRG_699t1:c.315-1536A>G	NP_000381.1:n.315-1536A>G
XM_006724615.2:c.252-1536A>G	XP_006724678.1:n.252-1536A>G
XM_011530839.1:c.-130-1536A>G	XP_011529141.1:n.-130-1536A>G
NM_000390.3:c.315-1536A>G	NP_000381.1:n.315-1536A>G
NM_001320959.1:c.-130-1536A>G	NP_001307888.1:n.-130-1536A>G
NM_001362517.1:c.-130-1536A>G	NP_001349446.1:n.-130-1536A>G
NM_001362518.1:c.-126-1540A>G	NP_001349447.1:n.-126-1540A>G
NM_001362519.1:c.-126-1540A>G	NP_001349448.1:n.-126-1540A>G
XM_017029242.2:c.315-1536A>G	XP_016884731.1:n.315-1536A>G
XM_017029246.1:c.-126-1540A>G	XP_016884735.1:n.-126-1540A>G
XM_024452331.1:c.-130-1536A>G	XP_024308099.1:n.-130-1536A>G
NM_000390.4:c.315-1536A>G MANE Select	NP_000381.1:n.315-1536A>G
NM_001362518.2:c.-126-1540A>G	NP_001349447.1:n.-126-1540A>G