Canonical Allele Identifier: CA2579655986
Gene: CHM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85956171del , CM000685.2:g.85956171del GRCh38
NC_000023.10:g.85211176del , CM000685.1:g.85211176del GRCh37
NC_000023.9:g.85097832del NCBI36
NG_009874.2:g.96392del , LRG_699:g.96392del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.1148del MANE Select ENSP00000350386.2:p.Leu383ProfsTer26
ENST00000357749.6:c.1148del ENSP00000350386.2:p.Leu383ProfsTer26
ENST00000467744.2:n.126+71320del
NM_000390.2:c.1148del , LRG_699t1:c.1148del NP_000381.1:p.Leu383ProfsTer26
XM_006724615.2:c.1085del XP_006724678.1:p.Leu362ProfsTer26
XM_011530839.1:c.704del XP_011529141.1:p.Leu235ProfsTer26
NM_000390.3:c.1148del NP_000381.1:p.Leu383ProfsTer26
NM_001320959.1:c.704del NP_001307888.1:p.Leu235ProfsTer26
NM_001362517.1:c.704del NP_001349446.1:p.Leu235ProfsTer26
NM_001362518.1:c.704del NP_001349447.1:p.Leu235ProfsTer26
NM_001362519.1:c.704del NP_001349448.1:p.Leu235ProfsTer26
XM_017029242.2:c.1148del XP_016884731.1:p.Leu383ProfsTer26
XM_017029246.1:c.704del XP_016884735.1:p.Leu235ProfsTer26
XM_024452331.1:c.704del XP_024308099.1:p.Leu235ProfsTer26
NM_000390.4:c.1148del MANE Select NP_000381.1:p.Leu383ProfsTer26
NM_001362518.2:c.704del NP_001349447.1:p.Leu235ProfsTer26