Canonical Allele Identifier: CA343316521

Gene: USF1

Linked Data

• MyVariant Identifiers: chr1:g.161013058C>A (hg19) ; chr1:g.161043268C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161043268C>A , CM000663.2:g.161043268C>A	GRCh38
NC_000001.10:g.161013058C>A , CM000663.1:g.161013058C>A	GRCh37
NC_000001.9:g.159279682C>A	NCBI36
NG_011612.1:g.7700G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368019.5:c.8G>T	ENSP00000356998.1:p.Gly3Val
ENST00000368020.5:c.8G>T	ENSP00000356999.1:p.Gly3Val
ENST00000368021.7:c.8G>T MANE Select	ENSP00000357000.3:p.Gly3Val
ENST00000473969.6:c.8G>T	ENSP00000435671.1:p.Gly3Val
ENST00000491629.5:n.144G>T
ENST00000496363.5:n.148G>T
ENST00000529476.1:n.175G>T
ENST00000531842.1:c.8G>T	ENSP00000435005.1:p.Gly3Val
ENST00000534633.5:c.-185G>T	ENSP00000432533.1:n.-185G>T
NM_001276373.1:c.8G>T	NP_001263302.1:p.Gly3Val
NM_007122.4:c.8G>T	NP_009053.1:p.Gly3Val
NM_207005.2:c.-139G>T	NP_996888.1:n.-139G>T
NM_007122.5:c.8G>T MANE Select	NP_009053.1:p.Gly3Val
NM_001276373.2:c.8G>T	NP_001263302.1:p.Gly3Val
NM_207005.3:c.-139G>T	NP_996888.1:n.-139G>T