Canonical Allele Identifier: CA1202576300

Gene: USF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161043242C= , CM000663.2:g.161043242C=	GRCh38
NC_000001.10:g.161013032C= , CM000663.1:g.161013032C=	GRCh37
NC_000001.9:g.159279656C=	NCBI36
NG_011612.1:g.7726G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368019.5:c.8+26G=	ENSP00000356998.1:n.8+26G=
ENST00000368020.5:c.8+26G=	ENSP00000356999.1:n.8+26G=
ENST00000368021.7:c.8+26G= MANE Select	ENSP00000357000.3:n.8+26G=
ENST00000473969.6:c.8+26G=	ENSP00000435671.1:n.8+26G=
ENST00000491629.5:n.144+26G=
ENST00000496363.5:n.148+26G=
ENST00000529476.1:n.175+26G=
ENST00000531842.1:c.8+26G=	ENSP00000435005.1:n.8+26G=
ENST00000534633.5:c.-170+11G=	ENSP00000432533.1:n.-170+11G=
NM_001276373.1:c.8+26G=	NP_001263302.1:n.8+26G=
NM_007122.4:c.8+26G=	NP_009053.1:n.8+26G=
NM_207005.2:c.-139+26G=	NP_996888.1:n.-139+26G=
NM_007122.5:c.8+26G= MANE Select	NP_009053.1:n.8+26G=
NM_001276373.2:c.8+26G=	NP_001263302.1:n.8+26G=
NM_207005.3:c.-139+26G=	NP_996888.1:n.-139+26G=