Canonical Allele Identifier: CA1139911857

Gene: USF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161040972C= , CM000663.2:g.161040972C=	GRCh38
NC_000001.10:g.161010762C= , CM000663.1:g.161010762C=	GRCh37
NC_000001.9:g.159277386C=	NCBI36
NG_011612.1:g.9996G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368019.5:c.477-100G=	ENSP00000356998.1:n.477-100G=
ENST00000368020.5:c.561-100G=	ENSP00000356999.1:n.561-100G=
ENST00000368021.7:c.561-100G= MANE Select	ENSP00000357000.3:n.561-100G=
ENST00000473969.6:c.*383-100G=	ENSP00000435671.1:n.*383-100G=
ENST00000496363.5:n.701-100G=
ENST00000528768.5:c.160-100G=
ENST00000531842.1:c.378-100G=	ENSP00000435005.1:n.378-100G=
NM_001276373.1:c.561-100G=	NP_001263302.1:n.561-100G=
NM_007122.4:c.561-100G=	NP_009053.1:n.561-100G=
NM_207005.2:c.384-100G=	NP_996888.1:n.384-100G=
NM_007122.5:c.561-100G= MANE Select	NP_009053.1:n.561-100G=
NM_001276373.2:c.561-100G=	NP_001263302.1:n.561-100G=
NM_207005.3:c.384-100G=	NP_996888.1:n.384-100G=