Canonical Allele Identifier: CA2442478019
Gene: CHM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85956203T= , CM000685.2:g.85956203T= GRCh38
NC_000023.10:g.85211208T= , CM000685.1:g.85211208T= GRCh37
NC_000023.9:g.85097864T= NCBI36
NG_009874.2:g.96360A= , LRG_699:g.96360A=

Transcript Alleles

HGVS Amino-acid change
ENST00000357749.7:c.1116A= MANE Select ENSP00000350386.2:p.Pro372=
ENST00000357749.6:c.1116A= ENSP00000350386.2:p.Pro372=
ENST00000467744.2:n.126+71288A=
NM_000390.2:c.1116A= , LRG_699t1:c.1116A= NP_000381.1:p.Pro372=
XM_006724615.2:c.1053A= XP_006724678.1:p.Pro351=
XM_011530839.1:c.672A= XP_011529141.1:p.Pro224=
NM_000390.3:c.1116A= NP_000381.1:p.Pro372=
NM_001320959.1:c.672A= NP_001307888.1:p.Pro224=
NM_001362517.1:c.672A= NP_001349446.1:p.Pro224=
NM_001362518.1:c.672A= NP_001349447.1:p.Pro224=
NM_001362519.1:c.672A= NP_001349448.1:p.Pro224=
XM_017029242.2:c.1116A= XP_016884731.1:p.Pro372=
XM_017029246.1:c.672A= XP_016884735.1:p.Pro224=
XM_024452331.1:c.672A= XP_024308099.1:p.Pro224=
NM_000390.4:c.1116A= MANE Select NP_000381.1:p.Pro372=
NM_001362518.2:c.672A= NP_001349447.1:p.Pro224=