Canonical Allele Identifier: CA2695234662
Gene: CHM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85956155del , CM000685.2:g.85956155del GRCh38
NC_000023.10:g.85211160del , CM000685.1:g.85211160del GRCh37
NC_000023.9:g.85097816del NCBI36
NG_009874.2:g.96408del , LRG_699:g.96408del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.1164del MANE Select ENSP00000350386.2:p.Cys388Ter
ENST00000357749.6:c.1164del ENSP00000350386.2:p.Cys388Ter
ENST00000467744.2:n.126+71336del
NM_000390.2:c.1164del , LRG_699t1:c.1164del NP_000381.1:p.Cys388Ter
XM_006724615.2:c.1101del XP_006724678.1:p.Cys367Ter
XM_011530839.1:c.720del XP_011529141.1:p.Cys240Ter
NM_000390.3:c.1164del NP_000381.1:p.Cys388Ter
NM_001320959.1:c.720del NP_001307888.1:p.Cys240Ter
NM_001362517.1:c.720del NP_001349446.1:p.Cys240Ter
NM_001362518.1:c.720del NP_001349447.1:p.Cys240Ter
NM_001362519.1:c.720del NP_001349448.1:p.Cys240Ter
XM_017029242.2:c.1164del XP_016884731.1:p.Cys388Ter
XM_017029246.1:c.720del XP_016884735.1:p.Cys240Ter
XM_024452331.1:c.720del XP_024308099.1:p.Cys240Ter
NM_000390.4:c.1164del MANE Select NP_000381.1:p.Cys388Ter
NM_001362518.2:c.720del NP_001349447.1:p.Cys240Ter