Canonical Allele Identifier: CA8084933

Gene: USB1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58014239G>A , CM000678.2:g.58014239G>A	GRCh38
NC_000016.9:g.58048143G>A , CM000678.1:g.58048143G>A	GRCh37
NC_000016.8:g.56605644G>A	NCBI36
NG_027698.1:g.17867G>A , LRG_352:g.17867G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561568.6:c.411-34G>A	ENSP00000457322.2:n.411-34G>A
ENST00000565662.6:c.450-34G>A	ENSP00000513729.1:n.450-34G>A
ENST00000698444.1:c.297-34G>A	ENSP00000513726.1:n.297-34G>A
ENST00000698445.1:c.450-34G>A	ENSP00000513727.1:n.450-34G>A
ENST00000698446.1:c.*195-3095G>A	ENSP00000513728.1:n.*195-3095G>A
ENST00000698447.1:c.*107-34G>A	ENSP00000513732.1:n.*107-34G>A
ENST00000219281.8:c.450-34G>A MANE Select	ENSP00000219281.3:n.450-34G>A
ENST00000219281.7:c.450-34G>A	ENSP00000219281.3:n.450-34G>A
ENST00000539737.6:c.450-3095G>A	ENSP00000446143.2:n.450-3095G>A
ENST00000561568.5:c.411-34G>A	ENSP00000457322.1:n.411-34G>A
ENST00000561743.5:c.297-34G>A	ENSP00000454928.1:n.297-34G>A
ENST00000562534.5:n.402-34G>A
ENST00000563207.1:n.326-34G>A
ENST00000564387.5:c.*107-34G>A	ENSP00000457302.1:n.*107-34G>A
ENST00000565151.1:n.611G>A
ENST00000565662.5:n.527-34G>A
ENST00000569252.5:n.536-34G>A
NM_001195302.1:c.450-3095G>A	NP_001182231.1:n.450-3095G>A
NM_024598.3:c.450-34G>A , LRG_352t1:c.450-34G>A	NP_078874.2:n.450-34G>A
XM_005256144.3:c.297-34G>A	XP_005256201.1:n.297-34G>A
XM_011523328.1:c.411-34G>A	XP_011521630.1:n.411-34G>A
XM_011523329.1:c.297-34G>A	XP_011521631.1:n.297-34G>A
NM_001330568.1:c.297-34G>A	NP_001317497.1:n.297-34G>A
NM_001195302.2:c.450-3095G>A	NP_001182231.1:n.450-3095G>A
NM_001330568.2:c.297-34G>A	NP_001317497.1:n.297-34G>A
NM_024598.4:c.450-34G>A MANE Select	NP_078874.2:n.450-34G>A