Canonical Allele Identifier: CA5058304

Gene: PAX5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37006458A>T , CM000671.2:g.37006458A>T	GRCh38
NC_000009.11:g.37006455A>T , CM000671.1:g.37006455A>T	GRCh37
NC_000009.10:g.36996455A>T	NCBI36
NG_033894.1:g.33022T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358127.9:c.475+15T>A MANE Select	ENSP00000350844.4:n.475+15T>A
ENST00000377852.7:c.475+15T>A	ENSP00000367083.2:n.475+15T>A
ENST00000520154.6:c.475+15T>A	ENSP00000429291.1:n.475+15T>A
ENST00000523241.6:c.475+15T>A	ENSP00000429637.1:n.475+15T>A
ENST00000651199.1:n.210-3682T>A
ENST00000651550.1:c.151+15T>A	ENSP00000498443.1:n.151+15T>A
ENST00000358127.8:c.475+15T>A	ENSP00000350844.4:n.475+15T>A
ENST00000377840.6:c.475+15T>A	ENSP00000367071.2:n.475+15T>A
ENST00000377847.6:c.475+15T>A	ENSP00000367078.2:n.475+15T>A
ENST00000377852.6:c.475+15T>A	ENSP00000367083.2:n.475+15T>A
ENST00000377853.6:c.475+15T>A	ENSP00000367084.2:n.475+15T>A
ENST00000414447.5:c.475+15T>A	ENSP00000412188.1:n.475+15T>A
ENST00000446742.5:c.277+15T>A	ENSP00000404687.1:n.277+15T>A
ENST00000520154.5:c.475+15T>A	ENSP00000429291.1:n.475+15T>A
ENST00000520281.5:c.475+15T>A	ENSP00000430773.1:n.475+15T>A
ENST00000522003.5:c.151+15T>A	ENSP00000429359.1:n.151+15T>A
ENST00000523145.5:c.151+15T>A	ENSP00000429197.1:n.151+15T>A
ENST00000523241.5:c.475+15T>A	ENSP00000429637.1:n.475+15T>A
ENST00000523493.5:c.475+15T>A	ENSP00000431038.1:n.475+15T>A
NM_001280547.1:c.475+15T>A	NP_001267476.1:n.475+15T>A
NM_001280548.1:c.475+15T>A	NP_001267477.1:n.475+15T>A
NM_001280549.1:c.475+15T>A	NP_001267478.1:n.475+15T>A
NM_001280550.1:c.475+15T>A	NP_001267479.1:n.475+15T>A
NM_001280551.1:c.151+15T>A	NP_001267480.1:n.151+15T>A
NM_001280552.1:c.475+15T>A	NP_001267481.1:n.475+15T>A
NM_001280553.1:c.475+15T>A	NP_001267482.1:n.475+15T>A
NM_001280554.1:c.475+15T>A	NP_001267483.1:n.475+15T>A
NM_001280555.1:c.277+15T>A	NP_001267484.1:n.277+15T>A
NM_001280556.1:c.151+15T>A	NP_001267485.1:n.151+15T>A
NM_016734.2:c.475+15T>A	NP_057953.1:n.475+15T>A
NR_103999.1:n.923+15T>A
NR_104000.1:n.923+15T>A
XM_005251481.3:c.472+15T>A	XP_005251538.1:n.472+15T>A
XM_011517896.1:c.475+15T>A	XP_011516198.1:n.475+15T>A
XM_011517897.1:c.472+15T>A	XP_011516199.1:n.472+15T>A
XR_929591.1:n.2216+445A>T
XR_929592.1:n.670+445A>T
XR_001746663.1:n.149-992A>T
XR_001746664.1:n.393+445A>T
XR_929591.2:n.2221+445A>T
NM_016734.3:c.475+15T>A MANE Select	NP_057953.1:n.475+15T>A
NM_001280547.2:c.475+15T>A	NP_001267476.1:n.475+15T>A
NM_001280548.2:c.475+15T>A	NP_001267477.1:n.475+15T>A
NM_001280549.2:c.475+15T>A	NP_001267478.1:n.475+15T>A
NM_001280550.2:c.475+15T>A	NP_001267479.1:n.475+15T>A
NM_001280551.2:c.151+15T>A	NP_001267480.1:n.151+15T>A
NM_001280552.2:c.475+15T>A	NP_001267481.1:n.475+15T>A
NM_001280553.2:c.475+15T>A	NP_001267482.1:n.475+15T>A
NM_001280554.2:c.475+15T>A	NP_001267483.1:n.475+15T>A
NM_001280555.2:c.277+15T>A	NP_001267484.1:n.277+15T>A
NM_001280556.2:c.151+15T>A	NP_001267485.1:n.151+15T>A
NR_103999.2:n.712+15T>A
NR_104000.2:n.712+15T>A