Canonical Allele Identifier: CA517490919

Gene: CHM

Linked Data

• ClinVar Variation Id: 1146804
• ClinVar RCV Id: RCV001486143
• dbSNP Id: rs1452326903
• gnomAD v2: X-85211169-C-T
• gnomAD v4: X-85956164-C-T
• MyVariant Identifiers: chrX:g.85211169C>T (hg19) ; chrX:g.85956164C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85956164C>T , CM000685.2:g.85956164C>T	GRCh38
NC_000023.10:g.85211169C>T , CM000685.1:g.85211169C>T	GRCh37
NC_000023.9:g.85097825C>T	NCBI36
NG_009874.2:g.96399G>A , LRG_699:g.96399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.1155G>A MANE Select	ENSP00000350386.2:p.Gln385=
ENST00000357749.6:c.1155G>A	ENSP00000350386.2:p.Gln385=
ENST00000467744.2:n.126+71327G>A
NM_000390.2:c.1155G>A , LRG_699t1:c.1155G>A	NP_000381.1:p.Gln385=
XM_006724615.2:c.1092G>A	XP_006724678.1:p.Gln364=
XM_011530839.1:c.711G>A	XP_011529141.1:p.Gln237=
NM_000390.3:c.1155G>A	NP_000381.1:p.Gln385=
NM_001320959.1:c.711G>A	NP_001307888.1:p.Gln237=
NM_001362517.1:c.711G>A	NP_001349446.1:p.Gln237=
NM_001362518.1:c.711G>A	NP_001349447.1:p.Gln237=
NM_001362519.1:c.711G>A	NP_001349448.1:p.Gln237=
XM_017029242.2:c.1155G>A	XP_016884731.1:p.Gln385=
XM_017029246.1:c.711G>A	XP_016884735.1:p.Gln237=
XM_024452331.1:c.711G>A	XP_024308099.1:p.Gln237=
NM_000390.4:c.1155G>A MANE Select	NP_000381.1:p.Gln385=
NM_001362518.2:c.711G>A	NP_001349447.1:p.Gln237=