Canonical Allele Identifier: CA413787682

Gene: CHM

Linked Data

• gnomAD v4: X-85879055-G-T
• MyVariant Identifiers: chrX:g.85134060G>T (hg19) ; chrX:g.85879055G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85879055G>T , CM000685.2:g.85879055G>T	GRCh38
NC_000023.10:g.85134060G>T , CM000685.1:g.85134060G>T	GRCh37
NC_000023.9:g.85020716G>T	NCBI36
NG_009874.2:g.173508C>A , LRG_699:g.173508C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.1519C>A MANE Select	ENSP00000350386.2:p.His507Asn
ENST00000357749.6:c.1519C>A	ENSP00000350386.2:p.His507Asn
ENST00000467744.2:n.127-15961C>A
NM_000390.2:c.1519C>A , LRG_699t1:c.1519C>A	NP_000381.1:p.His507Asn
XM_006724615.2:c.1456C>A	XP_006724678.1:p.His486Asn
XM_011530839.1:c.1075C>A	XP_011529141.1:p.His359Asn
NM_000390.3:c.1519C>A	NP_000381.1:p.His507Asn
NM_001320959.1:c.1075C>A	NP_001307888.1:p.His359Asn
NM_001362517.1:c.1075C>A	NP_001349446.1:p.His359Asn
NM_001362518.1:c.1075C>A	NP_001349447.1:p.His359Asn
NM_001362519.1:c.1075C>A	NP_001349448.1:p.His359Asn
XM_017029242.2:c.1519C>A	XP_016884731.1:p.His507Asn
XM_017029246.1:c.1075C>A	XP_016884735.1:p.His359Asn
XM_024452331.1:c.1075C>A	XP_024308099.1:p.His359Asn
NM_000390.4:c.1519C>A MANE Select	NP_000381.1:p.His507Asn
NM_001362518.2:c.1075C>A	NP_001349447.1:p.His359Asn