Canonical Allele Identifier: CA1202577022

Gene: USF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161044859A>C , CM000663.2:g.161044859A>C	GRCh38
NC_000001.10:g.161014649A>C , CM000663.1:g.161014649A>C	GRCh37
NC_000001.9:g.159281273A>C	NCBI36
NG_011612.1:g.6109T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_007122.5:c.-86+999T>G MANE Select	NP_009053.1:n.-86+999T>G
ENST00000368021.7:c.-86+999T>G MANE Select	ENSP00000357000.3:n.-86+999T>G
NM_001276373.1:c.-86+53T>G	NP_001263302.1:n.-86+53T>G
NM_001276373.2:c.-86+53T>G	NP_001263302.1:n.-86+53T>G
NM_007122.4:c.-86+999T>G	NP_009053.1:n.-86+999T>G
NM_207005.2:c.-232+999T>G	NP_996888.1:n.-232+999T>G
NM_207005.3:c.-232+999T>G	NP_996888.1:n.-232+999T>G
ENST00000368020.5:c.-86+53T>G	ENSP00000356999.1:n.-86+53T>G
ENST00000473969.6:c.-86+999T>G	ENSP00000435671.1:n.-86+999T>G
ENST00000491629.5:n.51+999T>G
ENST00000496363.5:n.55+999T>G
ENST00000529476.1:n.82+999T>G
ENST00000534633.5:c.-278+999T>G	ENSP00000432533.1:n.-278+999T>G