Canonical Allele Identifier: CA2574429831
Gene: HFM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91266065dup , CM000663.2:g.91266065dup GRCh38
NC_000001.10:g.91731622dup , CM000663.1:g.91731622dup GRCh37
NC_000001.9:g.91504210dup NCBI36
NG_034120.1:g.143805dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370425.8:c.3926dup MANE Select ENSP00000359454.3:p.Pro1310ThrfsTer22
ENST00000370425.7:c.3926dup ENSP00000359454.3:p.Pro1310ThrfsTer22
ENST00000430465.1:c.1561dup
ENST00000462405.5:n.1809+1680dup
NM_001017975.4:c.3926dup NP_001017975.4:p.Pro1310ThrfsTer22
XM_006710395.2:c.2159dup XP_006710458.1:p.Pro721ThrfsTer22
XM_011540847.1:c.3923dup XP_011539149.1:p.Pro1309ThrfsTer22
XM_011540848.1:c.3845dup XP_011539150.1:p.Pro1283ThrfsTer22
XM_011540849.1:c.3926dup XP_011539151.1:p.Pro1310ThrfsTer22
XM_011540850.1:c.3926dup XP_011539152.1:p.Pro1310ThrfsTer22
XM_011540851.1:c.3926dup XP_011539153.1:p.Pro1310ThrfsTer22
XM_011540852.1:c.3926dup XP_011539154.1:p.Pro1310ThrfsTer22
XM_011540853.1:c.3794dup XP_011539155.1:p.Pro1266ThrfsTer22
XM_011540854.1:c.3926dup XP_011539156.1:p.Pro1310ThrfsTer?
XM_011540855.1:c.3800dup XP_011539157.1:p.Pro1268ThrfsTer22
XM_011540856.1:c.3883+1680dup XP_011539158.1:n.3883+1680dup
XM_011540857.1:c.3503dup XP_011539159.1:p.Pro1169ThrfsTer22
XM_011540858.1:c.2963dup XP_011539160.1:p.Pro989ThrfsTer22
XM_011540859.1:c.2753dup XP_011539161.1:p.Pro919ThrfsTer22
XM_011540850.2:c.3926dup XP_011539152.1:p.Pro1310ThrfsTer22
XM_011540852.2:c.3926dup XP_011539154.1:p.Pro1310ThrfsTer22
XM_011540855.2:c.3800dup XP_011539157.1:p.Pro1268ThrfsTer22
XM_011540859.2:c.2753dup XP_011539161.1:p.Pro919ThrfsTer22
XM_017000490.1:c.3845dup XP_016855979.1:p.Pro1283ThrfsTer22
XM_017000491.1:c.3794dup XP_016855980.1:p.Pro1266ThrfsTer22
XM_017000492.1:c.2963dup XP_016855981.1:p.Pro989ThrfsTer22
XM_017000493.1:c.2255dup XP_016855982.1:p.Pro753ThrfsTer22
XR_001737008.1:n.3926+1680dup
XR_001737009.1:n.3840+1680dup
XR_001737010.1:n.3708+1680dup
NM_001017975.5:c.3926dup NP_001017975.4:p.Pro1310ThrfsTer22
NM_001017975.6:c.3926dup MANE Select NP_001017975.5:p.Pro1310ThrfsTer22
NR_165455.1:n.3516dup