Canonical Allele Identifier: CA1202576348

Gene: USF1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161043351G= , CM000663.2:g.161043351G=	GRCh38
NC_000001.10:g.161013141G= , CM000663.1:g.161013141G=	GRCh37
NC_000001.9:g.159279765G=	NCBI36
NG_011612.1:g.7617C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368019.5:c.-76C=	ENSP00000356998.1:n.-76C=
ENST00000368020.5:c.-76C=	ENSP00000356999.1:n.-76C=
ENST00000368021.7:c.-76C= MANE Select	ENSP00000357000.3:n.-76C=
ENST00000473969.6:c.-76C=	ENSP00000435671.1:n.-76C=
ENST00000491629.5:n.61C=
ENST00000496363.5:n.65C=
ENST00000529476.1:n.92C=
ENST00000534633.5:c.-268C=	ENSP00000432533.1:n.-268C=
NM_001276373.1:c.-76C=	NP_001263302.1:n.-76C=
NM_007122.4:c.-76C=	NP_009053.1:n.-76C=
NM_207005.2:c.-222C=	NP_996888.1:n.-222C=
NM_007122.5:c.-76C= MANE Select	NP_009053.1:n.-76C=
NM_001276373.2:c.-76C=	NP_001263302.1:n.-76C=
NM_207005.3:c.-222C=	NP_996888.1:n.-222C=