Canonical Allele Identifier: CA890169336

Gene: USF1

Genomic Alleles

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

Transcript Alleles

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