Canonical Allele Identifier: CA2580584352

Gene: USF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161043331C>A , CM000663.2:g.161043331C>A	GRCh38
NC_000001.10:g.161013121C>A , CM000663.1:g.161013121C>A	GRCh37
NC_000001.9:g.159279745C>A	NCBI36
NG_011612.1:g.7637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368019.5:c.-56G>T	ENSP00000356998.1:n.-56G>T
ENST00000368020.5:c.-56G>T	ENSP00000356999.1:n.-56G>T
ENST00000368021.7:c.-56G>T MANE Select	ENSP00000357000.3:n.-56G>T
ENST00000473969.6:c.-56G>T	ENSP00000435671.1:n.-56G>T
ENST00000491629.5:n.81G>T
ENST00000496363.5:n.85G>T
ENST00000529476.1:n.112G>T
ENST00000531842.1:c.-56G>T	ENSP00000435005.1:n.-56G>T
ENST00000534633.5:c.-248G>T	ENSP00000432533.1:n.-248G>T
NM_001276373.1:c.-56G>T	NP_001263302.1:n.-56G>T
NM_007122.4:c.-56G>T	NP_009053.1:n.-56G>T
NM_207005.2:c.-202G>T	NP_996888.1:n.-202G>T
NM_007122.5:c.-56G>T MANE Select	NP_009053.1:n.-56G>T
NM_001276373.2:c.-56G>T	NP_001263302.1:n.-56G>T
NM_207005.3:c.-202G>T	NP_996888.1:n.-202G>T