Canonical Allele Identifier: CA1509555344
Gene: MARCHF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.164300819G= , CM000666.2:g.164300819G= GRCh38
NC_000004.11:g.165221971G= , CM000666.1:g.165221971G= GRCh37
NC_000004.10:g.165441421G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001394959.1:c.-323+83051C= MANE Select NP_001381888.1:n.-323+83051C=
ENST00000514618.6:c.-323+83051C= MANE Select ENSP00000421322.1:n.-323+83051C=
NM_001166373.1:c.-114+82368C= NP_001159845.1:n.-114+82368C=
NM_001166373.2:c.-114+82368C= NP_001159845.1:n.-114+82368C=
ENST00000503008.5:c.-114+82368C= ENSP00000427223.1:n.-114+82368C=
ENST00000505391.5:n.311+29111C=
ENST00000507270.5:c.-114+83051C= ENSP00000426731.1:n.-114+83051C=
ENST00000508725.5:n.332-65903C=
ENST00000510075.1:n.331+82368C=
ENST00000514618.5:c.-323+83051C= ENSP00000421322.1:n.-323+83051C=
ENST00000515471.5:n.380+82368C=
XM_011532056.1:c.-114+83051C= XP_011530358.1:n.-114+83051C=
XM_017008335.1:c.-186+82368C= XP_016863824.1:n.-186+82368C=
XM_017008336.1:c.-186+83051C= XP_016863825.1:n.-186+83051C=