Canonical Allele Identifier: CA1202576345
Gene: USF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161043349G= , CM000663.2:g.161043349G= GRCh38
NC_000001.10:g.161013139G= , CM000663.1:g.161013139G= GRCh37
NC_000001.9:g.159279763G= NCBI36
NG_011612.1:g.7619C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368019.5:c.-74C= ENSP00000356998.1:n.-74C=
ENST00000368020.5:c.-74C= ENSP00000356999.1:n.-74C=
ENST00000368021.7:c.-74C= MANE Select ENSP00000357000.3:n.-74C=
ENST00000473969.6:c.-74C= ENSP00000435671.1:n.-74C=
ENST00000491629.5:n.63C=
ENST00000496363.5:n.67C=
ENST00000529476.1:n.94C=
ENST00000534633.5:c.-266C= ENSP00000432533.1:n.-266C=
NM_001276373.1:c.-74C= NP_001263302.1:n.-74C=
NM_007122.4:c.-74C= NP_009053.1:n.-74C=
NM_207005.2:c.-220C= NP_996888.1:n.-220C=
NM_007122.5:c.-74C= MANE Select NP_009053.1:n.-74C=
NM_001276373.2:c.-74C= NP_001263302.1:n.-74C=
NM_207005.3:c.-220C= NP_996888.1:n.-220C=