Canonical Allele Identifier: CA1139955624
Gene: USF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161041926G= , CM000663.2:g.161041926G= GRCh38
NC_000001.10:g.161011716G= , CM000663.1:g.161011716G= GRCh37
NC_000001.9:g.159278340G= NCBI36
NG_011612.1:g.9042C=

Transcript Alleles

HGVS Amino-acid Change
NM_007122.5:c.277-80C= MANE Select NP_009053.1:n.277-80C=
ENST00000368021.7:c.277-80C= MANE Select ENSP00000357000.3:n.277-80C=
NM_001276373.1:c.277-80C= NP_001263302.1:n.277-80C=
NM_001276373.2:c.277-80C= NP_001263302.1:n.277-80C=
NM_007122.4:c.277-80C= NP_009053.1:n.277-80C=
NM_207005.2:c.100-80C= NP_996888.1:n.100-80C=
NM_207005.3:c.100-80C= NP_996888.1:n.100-80C=
ENST00000368019.5:c.277-80C= ENSP00000356998.1:n.277-80C=
ENST00000368020.5:c.277-80C= ENSP00000356999.1:n.277-80C=
ENST00000473969.6:c.*99-80C= ENSP00000435671.1:n.*99-80C=
ENST00000491629.5:n.413-80C=
ENST00000496363.5:n.417-80C=
ENST00000529476.1:n.342-80C=
ENST00000531842.1:c.277-80C= ENSP00000435005.1:n.277-80C=
ENST00000534633.5:c.100-80C= ENSP00000432533.1:n.100-80C=