Canonical Allele Identifier: CA1139661974

Gene: FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61967561G>T , CM000673.2:g.61967561G>T	GRCh38
NC_000011.9:g.61735033G>T , CM000673.1:g.61735033G>T	GRCh37
NC_000011.8:g.61491609G>T	NCBI36
NG_008346.1:g.5100C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002032.3:c.-136C>A MANE Select	NP_002023.2:n.-136C>A
ENST00000273550.12:c.-136C>A MANE Select	ENSP00000273550.7:n.-136C>A
NM_002032.2:c.-136C>A	NP_002023.2:n.-136C>A
ENST00000273550.11:c.-136C>A	ENSP00000273550.7:n.-136C>A
ENST00000526640.5:c.-136C>A	ENSP00000433321.1:n.-136C>A
ENST00000529191.5:c.-136C>A	ENSP00000431659.1:n.-136C>A
ENST00000529548.1:c.-322C>A	ENSP00000436947.1:n.-322C>A
ENST00000529631.5:c.-136C>A	ENSP00000431575.1:n.-136C>A
ENST00000530019.5:c.-136C>A	ENSP00000433470.1:n.-136C>A
ENST00000532829.5:c.-136C>A	ENSP00000432223.1:n.-136C>A
ENST00000533138.1:n.53C>A
ENST00000534180.1:c.-136C>A	ENSP00000434403.1:n.-136C>A
ENST00000534719.1:n.26C>A
ENST00000620041.4:c.-42C>A	ENSP00000484477.1:n.-42C>A
ENST00000620041.5:c.-47C>A	ENSP00000484477.1:n.-47C>A