Canonical Allele Identifier: CA2580584346
Gene: USF1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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