Canonical Allele Identifier: CA1140466108
Gene: USF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161040986G= , CM000663.2:g.161040986G= GRCh38
NC_000001.10:g.161010776G= , CM000663.1:g.161010776G= GRCh37
NC_000001.9:g.159277400G= NCBI36
NG_011612.1:g.9982C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368019.5:c.477-114C= ENSP00000356998.1:n.477-114C=
ENST00000368020.5:c.561-114C= ENSP00000356999.1:n.561-114C=
ENST00000368021.7:c.561-114C= MANE Select ENSP00000357000.3:n.561-114C=
ENST00000473969.6:c.*383-114C= ENSP00000435671.1:n.*383-114C=
ENST00000496363.5:n.701-114C=
ENST00000528768.5:c.160-114C=
ENST00000531842.1:c.378-114C= ENSP00000435005.1:n.378-114C=
NM_001276373.1:c.561-114C= NP_001263302.1:n.561-114C=
NM_007122.4:c.561-114C= NP_009053.1:n.561-114C=
NM_207005.2:c.384-114C= NP_996888.1:n.384-114C=
NM_007122.5:c.561-114C= MANE Select NP_009053.1:n.561-114C=
NM_001276373.2:c.561-114C= NP_001263302.1:n.561-114C=
NM_207005.3:c.384-114C= NP_996888.1:n.384-114C=