Canonical Allele Identifier: CA1977539548

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61964988T= , CM000673.2:g.61964988T= GRCh38
NC_000011.9:g.61732460T= , CM000673.1:g.61732460T= GRCh37
NC_000011.8:g.61489036T= NCBI36
NG_008346.1:g.7673A=
NG_009033.1:g.20105T=

Transcript Alleles

HGVS Amino-acid change
ENST00000620041.5:c.386A= (FTH1) ENSP00000484477.1:p.His129=
ENST00000273550.12:c.386A= (FTH1) MANE Select ENSP00000273550.7:p.His129=
ENST00000273550.11:c.386A= (FTH1) ENSP00000273550.7:p.His129=
ENST00000449131.6:c.*1839T= (BEST1) ENSP00000399709.2:n.*1839T=
ENST00000526640.5:c.296A= (FTH1) ENSP00000433321.1:p.His99=
ENST00000529191.5:c.114+2324A= (FTH1) ENSP00000431659.1:n.114+2324A=
ENST00000529631.5:c.114+2324A= (FTH1) ENSP00000431575.1:n.114+2324A=
ENST00000530019.5:c.261+381A= (FTH1) ENSP00000433470.1:n.261+381A=
ENST00000532601.1:c.176A= (FTH1) ENSP00000435111.1:p.His59=
ENST00000532829.5:c.*91A= (FTH1) ENSP00000432223.1:n.*91A=
ENST00000533138.1:n.830A= (FTH1)
ENST00000534180.1:c.*295A= (FTH1) ENSP00000434403.1:n.*295A=
ENST00000534719.1:n.547A= (FTH1)
ENST00000620041.4:c.386A= (FTH1) ENSP00000484477.1:p.His129=
NM_002032.2:c.386A= (FTH1) NP_002023.2:p.His129=
NM_002032.3:c.386A= (FTH1) MANE Select NP_002023.2:p.His129=
NM_001139443.2:c.*1839T= (BEST1) NP_001132915.1:n.*1839T=
NM_001363591.2:c.*1839T= (BEST1) NP_001350520.1:n.*1839T=
NM_001363593.2:c.*1839T= (BEST1) NP_001350522.1:n.*1839T=