Canonical Allele Identifier: CA863687364

Gene: PAX5

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36969208G>C , CM000671.2:g.36969208G>C	GRCh38
NC_000009.11:g.36969205G>C , CM000671.1:g.36969205G>C	GRCh37
NC_000009.10:g.36959205G>C	NCBI36
NG_033894.1:g.70272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358127.9:c.605-2484C>G MANE Select	ENSP00000350844.4:n.605-2484C>G
ENST00000377852.7:c.605-2484C>G	ENSP00000367083.2:n.605-2484C>G
ENST00000520154.6:c.605-2484C>G	ENSP00000429291.1:n.605-2484C>G
ENST00000523241.6:c.605-2484C>G	ENSP00000429637.1:n.605-2484C>G
ENST00000651550.1:c.281-2484C>G	ENSP00000498443.1:n.281-2484C>G
ENST00000358127.8:c.605-2484C>G	ENSP00000350844.4:n.605-2484C>G
ENST00000377840.6:c.605-2484C>G	ENSP00000367071.2:n.605-2484C>G
ENST00000377847.6:c.605-2484C>G	ENSP00000367078.2:n.605-2484C>G
ENST00000377852.6:c.605-2484C>G	ENSP00000367083.2:n.605-2484C>G
ENST00000377853.6:c.605-2484C>G	ENSP00000367084.2:n.605-2484C>G
ENST00000414447.5:c.476-2484C>G	ENSP00000412188.1:n.476-2484C>G
ENST00000446742.5:c.407-2484C>G	ENSP00000404687.1:n.407-2484C>G
ENST00000520154.5:c.605-2484C>G	ENSP00000429291.1:n.605-2484C>G
ENST00000520281.5:c.476-2484C>G	ENSP00000430773.1:n.476-2484C>G
ENST00000522003.5:c.281-2484C>G	ENSP00000429359.1:n.281-2484C>G
ENST00000522932.1:c.105+33440C>G
ENST00000523145.5:c.281-2484C>G	ENSP00000429197.1:n.281-2484C>G
ENST00000523241.5:c.605-2484C>G	ENSP00000429637.1:n.605-2484C>G
ENST00000523493.5:c.605-2484C>G	ENSP00000431038.1:n.605-2484C>G
ENST00000524340.5:c.29-2484C>G	ENSP00000429404.1:n.29-2484C>G
NM_001280547.1:c.605-2484C>G	NP_001267476.1:n.605-2484C>G
NM_001280548.1:c.605-2484C>G	NP_001267477.1:n.605-2484C>G
NM_001280549.1:c.605-2484C>G	NP_001267478.1:n.605-2484C>G
NM_001280550.1:c.605-2484C>G	NP_001267479.1:n.605-2484C>G
NM_001280551.1:c.281-2484C>G	NP_001267480.1:n.281-2484C>G
NM_001280552.1:c.605-2484C>G	NP_001267481.1:n.605-2484C>G
NM_001280553.1:c.476-2484C>G	NP_001267482.1:n.476-2484C>G
NM_001280554.1:c.476-2484C>G	NP_001267483.1:n.476-2484C>G
NM_001280555.1:c.407-2484C>G	NP_001267484.1:n.407-2484C>G
NM_001280556.1:c.281-2484C>G	NP_001267485.1:n.281-2484C>G
NM_016734.2:c.605-2484C>G	NP_057953.1:n.605-2484C>G
NR_103999.1:n.1053-2484C>G
NR_104000.1:n.1053-2484C>G
XM_005251481.3:c.602-2484C>G	XP_005251538.1:n.602-2484C>G
XM_011517896.1:c.605-2484C>G	XP_011516198.1:n.605-2484C>G
XM_011517897.1:c.602-2484C>G	XP_011516199.1:n.602-2484C>G
NM_016734.3:c.605-2484C>G MANE Select	NP_057953.1:n.605-2484C>G
NM_001280547.2:c.605-2484C>G	NP_001267476.1:n.605-2484C>G
NM_001280548.2:c.605-2484C>G	NP_001267477.1:n.605-2484C>G
NM_001280549.2:c.605-2484C>G	NP_001267478.1:n.605-2484C>G
NM_001280550.2:c.605-2484C>G	NP_001267479.1:n.605-2484C>G
NM_001280551.2:c.281-2484C>G	NP_001267480.1:n.281-2484C>G
NM_001280552.2:c.605-2484C>G	NP_001267481.1:n.605-2484C>G
NM_001280553.2:c.476-2484C>G	NP_001267482.1:n.476-2484C>G
NM_001280554.2:c.476-2484C>G	NP_001267483.1:n.476-2484C>G
NM_001280555.2:c.407-2484C>G	NP_001267484.1:n.407-2484C>G
NM_001280556.2:c.281-2484C>G	NP_001267485.1:n.281-2484C>G
NR_103999.2:n.842-2484C>G
NR_104000.2:n.842-2484C>G