Canonical Allele Identifier: CA2648728319

Gene: USF1

Linked Data

• gnomAD v4: 1-161040990-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161040990G>A , CM000663.2:g.161040990G>A	GRCh38
NC_000001.10:g.161010780G>A , CM000663.1:g.161010780G>A	GRCh37
NC_000001.9:g.159277404G>A	NCBI36
NG_011612.1:g.9978C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368019.5:c.477-118C>T	ENSP00000356998.1:n.477-118C>T
ENST00000368020.5:c.561-118C>T	ENSP00000356999.1:n.561-118C>T
ENST00000368021.7:c.561-118C>T MANE Select	ENSP00000357000.3:n.561-118C>T
ENST00000473969.6:c.*383-118C>T	ENSP00000435671.1:n.*383-118C>T
ENST00000496363.5:n.701-118C>T
ENST00000528768.5:c.160-118C>T
ENST00000531842.1:c.378-118C>T	ENSP00000435005.1:n.378-118C>T
NM_001276373.1:c.561-118C>T	NP_001263302.1:n.561-118C>T
NM_007122.4:c.561-118C>T	NP_009053.1:n.561-118C>T
NM_207005.2:c.384-118C>T	NP_996888.1:n.384-118C>T
NM_007122.5:c.561-118C>T MANE Select	NP_009053.1:n.561-118C>T
NM_001276373.2:c.561-118C>T	NP_001263302.1:n.561-118C>T
NM_207005.3:c.384-118C>T	NP_996888.1:n.384-118C>T