Canonical Allele Identifier: CA373487166

Gene: PAX5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36882057G>C , CM000671.2:g.36882057G>C	GRCh38
NC_000009.11:g.36882054G>C , CM000671.1:g.36882054G>C	GRCh37
NC_000009.10:g.36872054G>C	NCBI36
NG_033894.1:g.157423C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358127.9:c.959C>G MANE Select	ENSP00000350844.4:p.Pro320Arg
ENST00000377852.7:c.911-35128C>G	ENSP00000367083.2:n.911-35128C>G
ENST00000520154.6:c.781-41421C>G	ENSP00000429291.1:n.781-41421C>G
ENST00000523241.6:c.781-35128C>G	ENSP00000429637.1:n.781-35128C>G
ENST00000651550.1:c.635C>G	ENSP00000498443.1:p.Pro212Arg
ENST00000358127.8:c.959C>G	ENSP00000350844.4:p.Pro320Arg
ENST00000377840.6:c.829C>G	ENSP00000367071.2:p.Pro277Ala
ENST00000377847.6:c.910+41298C>G	ENSP00000367078.2:n.910+41298C>G
ENST00000377852.6:c.911-35128C>G	ENSP00000367083.2:n.911-35128C>G
ENST00000377853.6:c.959C>G	ENSP00000367084.2:p.Pro320Arg
ENST00000414447.5:c.830C>G	ENSP00000412188.1:p.Pro277Arg
ENST00000446742.5:c.713-35128C>G	ENSP00000404687.1:n.713-35128C>G
ENST00000520154.5:c.781-41421C>G	ENSP00000429291.1:n.781-41421C>G
ENST00000520281.5:c.830C>G	ENSP00000430773.1:p.Pro277Arg
ENST00000522003.5:c.635C>G	ENSP00000429359.1:p.Pro212Arg
ENST00000522932.1:c.106-41421C>G
ENST00000523145.5:c.586+41298C>G	ENSP00000429197.1:n.586+41298C>G
ENST00000523241.5:c.781-35128C>G	ENSP00000429637.1:n.781-35128C>G
ENST00000523493.5:c.886C>G	ENSP00000431038.1:p.Pro296Ala
ENST00000524340.5:c.440C>G	ENSP00000429404.1:p.Pro147Arg
NM_001280547.1:c.911-35128C>G	NP_001267476.1:n.911-35128C>G
NM_001280548.1:c.959C>G	NP_001267477.1:p.Pro320Arg
NM_001280549.1:c.781-35128C>G	NP_001267478.1:n.781-35128C>G
NM_001280550.1:c.781-41421C>G	NP_001267479.1:n.781-41421C>G
NM_001280551.1:c.586+41298C>G	NP_001267480.1:n.586+41298C>G
NM_001280552.1:c.910+41298C>G	NP_001267481.1:n.910+41298C>G
NM_001280553.1:c.830C>G	NP_001267482.1:p.Pro277Arg
NM_001280554.1:c.830C>G	NP_001267483.1:p.Pro277Arg
NM_001280555.1:c.713-35128C>G	NP_001267484.1:n.713-35128C>G
NM_001280556.1:c.635C>G	NP_001267485.1:p.Pro212Arg
NM_016734.2:c.959C>G	NP_057953.1:p.Pro320Arg
NR_103999.1:n.1277C>G
NR_104000.1:n.1334C>G
XM_005251481.3:c.956C>G	XP_005251538.1:p.Pro319Arg
XM_011517896.1:c.1016C>G	XP_011516198.1:p.Pro339Arg
XM_011517897.1:c.1013C>G	XP_011516199.1:p.Pro338Arg
NM_016734.3:c.959C>G MANE Select	NP_057953.1:p.Pro320Arg
NM_001280547.2:c.911-35128C>G	NP_001267476.1:n.911-35128C>G
NM_001280548.2:c.959C>G	NP_001267477.1:p.Pro320Arg
NM_001280549.2:c.781-35128C>G	NP_001267478.1:n.781-35128C>G
NM_001280550.2:c.781-41421C>G	NP_001267479.1:n.781-41421C>G
NM_001280551.2:c.586+41298C>G	NP_001267480.1:n.586+41298C>G
NM_001280552.2:c.910+41298C>G	NP_001267481.1:n.910+41298C>G
NM_001280553.2:c.830C>G	NP_001267482.1:p.Pro277Arg
NM_001280554.2:c.830C>G	NP_001267483.1:p.Pro277Arg
NM_001280555.2:c.713-35128C>G	NP_001267484.1:n.713-35128C>G
NM_001280556.2:c.635C>G	NP_001267485.1:p.Pro212Arg
NR_103999.2:n.1066C>G
NR_104000.2:n.1123C>G