Canonical Allele Identifier: CA413786541
Gene: CHM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.85963748T>A , CM000685.2:g.85963748T>A GRCh38
NC_000023.10:g.85218753T>A , CM000685.1:g.85218753T>A GRCh37
NC_000023.9:g.85105409T>A NCBI36
NG_009874.2:g.88815A>T , LRG_699:g.88815A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357749.7:c.619A>T MANE Select ENSP00000350386.2:p.Thr207Ser
ENST00000357749.6:c.619A>T ENSP00000350386.2:p.Thr207Ser
ENST00000467744.2:n.126+63743A>T
NM_000390.2:c.619A>T , LRG_699t1:c.619A>T NP_000381.1:p.Thr207Ser
XM_006724615.2:c.556A>T XP_006724678.1:p.Thr186Ser
XM_011530839.1:c.175A>T XP_011529141.1:p.Thr59Ser
NM_000390.3:c.619A>T NP_000381.1:p.Thr207Ser
NM_001320959.1:c.175A>T NP_001307888.1:p.Thr59Ser
NM_001362517.1:c.175A>T NP_001349446.1:p.Thr59Ser
NM_001362518.1:c.175A>T NP_001349447.1:p.Thr59Ser
NM_001362519.1:c.175A>T NP_001349448.1:p.Thr59Ser
XM_017029242.2:c.619A>T XP_016884731.1:p.Thr207Ser
XM_017029246.1:c.175A>T XP_016884735.1:p.Thr59Ser
XM_024452331.1:c.175A>T XP_024308099.1:p.Thr59Ser
NM_000390.4:c.619A>T MANE Select NP_000381.1:p.Thr207Ser
NM_001362518.2:c.175A>T NP_001349447.1:p.Thr59Ser