Canonical Allele Identifier: CA2648728326

Gene: USF1

Linked Data

• gnomAD v4: 1-161040992-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161040992T>C , CM000663.2:g.161040992T>C	GRCh38
NC_000001.10:g.161010782T>C , CM000663.1:g.161010782T>C	GRCh37
NC_000001.9:g.159277406T>C	NCBI36
NG_011612.1:g.9976A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368019.5:c.477-120A>G	ENSP00000356998.1:n.477-120A>G
ENST00000368020.5:c.561-120A>G	ENSP00000356999.1:n.561-120A>G
ENST00000368021.7:c.561-120A>G MANE Select	ENSP00000357000.3:n.561-120A>G
ENST00000473969.6:c.*383-120A>G	ENSP00000435671.1:n.*383-120A>G
ENST00000496363.5:n.701-120A>G
ENST00000528768.5:c.160-120A>G
ENST00000531842.1:c.378-120A>G	ENSP00000435005.1:n.378-120A>G
NM_001276373.1:c.561-120A>G	NP_001263302.1:n.561-120A>G
NM_007122.4:c.561-120A>G	NP_009053.1:n.561-120A>G
NM_207005.2:c.384-120A>G	NP_996888.1:n.384-120A>G
NM_007122.5:c.561-120A>G MANE Select	NP_009053.1:n.561-120A>G
NM_001276373.2:c.561-120A>G	NP_001263302.1:n.561-120A>G
NM_207005.3:c.384-120A>G	NP_996888.1:n.384-120A>G