Canonical Allele Identifier: CA395960970
Community Standard Title: NM_001144.6(AMFR):c.978T>A (p.Phe326Leu)
Gene: AMFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56401840A>T , CM000678.2:g.56401840A>T GRCh38
NC_000016.9:g.56435752A>T , CM000678.1:g.56435752A>T GRCh37
NC_000016.8:g.54993253A>T NCBI36
NG_047034.1:g.28699T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001144.6:c.978T>A MANE Select NP_001135.3:p.Phe326Leu
ENST00000290649.10:c.978T>A MANE Select ENSP00000290649.5:p.Phe326Leu
NM_001144.5:c.978T>A NP_001135.3:p.Phe326Leu
NM_001323511.1:c.693T>A NP_001310440.1:p.Phe231Leu
NM_001323511.2:c.693T>A NP_001310440.1:p.Phe231Leu
NM_001323512.1:c.978T>A NP_001310441.1:p.Phe326Leu
NM_001323512.2:c.978T>A NP_001310441.1:p.Phe326Leu
ENST00000290649.9:c.978T>A ENSP00000290649.5:p.Phe326Leu
ENST00000492830.5:c.137T>A ENSP00000473636.1:p.Leu46Ter
ENST00000567738.1:c.123T>A ENSP00000456288.1:p.Phe41Leu
XM_005255889.2:c.693T>A XP_005255946.1:p.Phe231Leu
XM_005255890.2:c.693T>A XP_005255947.1:p.Phe231Leu
XM_005255890.4:c.693T>A XP_005255947.1:p.Phe231Leu