Canonical Allele Identifier: CA1139880066

Gene: USF1

Genomic Alleles

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

Transcript Alleles

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