Canonical Allele Identifier: CA2763074935

Gene: PITX2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110621397_110621398insACAACAAAACCCAAACACAC , CM000666.2:g.110621397_110621398insACAACAAAACCCAAACACAC	GRCh38
NC_000004.11:g.111542553_111542554insACAACAAAACCCAAACACAC , CM000666.1:g.111542553_111542554insACAACAAAACCCAAACACAC	GRCh37
NC_000004.10:g.111762002_111762003insACAACAAAACCCAAACACAC	NCBI36
NG_007120.1:g.20955_20956insGTGTGTTTGGGTTTTGTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.185-2710_185-2709insGTGTGTTTGGGTTTTGTTGT	ENSP00000484763.2:n.185-2710_185-2709insGTGTGTTTGGGTTTTGTTGT
ENST00000614423.5:c.104-29_104-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000481951.2:n.104-29_104-28insGTGTGTTTGGGTTTTGTTGT
ENST00000616641.5:n.172-29_172-28insGTGTGTTTGGGTTTTGTTGT
ENST00000644488.2:n.176-29_176-28insGTGTGTTTGGGTTTTGTTGT
ENST00000394595.8:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000378095.4:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000644488.1:n.248-29_248-28insGTGTGTTTGGGTTTTGTTGT
ENST00000644743.1:c.206-29_206-28insGTGTGTTTGGGTTTTGTTGT MANE Select	ENSP00000495061.1:n.206-29_206-28insGTGTGTTTGGGTTTTGTTGT
ENST00000645131.1:n.137-29_137-28insGTGTGTTTGGGTTTTGTTGT
ENST00000306732.7:c.206-29_206-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000304169.3:n.206-29_206-28insGTGTGTTTGGGTTTTGTTGT
ENST00000354925.6:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000347004.2:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000355080.9:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000347192.5:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
ENST00000394595.7:c.185-2710_185-2709insGTGTGTTTGGGTTTTGTTGT	ENSP00000378095.3:n.185-2710_185-2709insGTGTGTTTGGGTTTTGTTGT
ENST00000394598.6:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000378097.2:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000511837.5:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000421454.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000511990.1:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000424142.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
ENST00000557119.2:c.206-29_206-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000475617.1:n.206-29_206-28insGTGTGTTTGGGTTTTGTTGT
ENST00000613094.4:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000484763.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000614423.4:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000481951.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
ENST00000616641.4:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	ENSP00000484909.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
NM_000325.5:c.206-29_206-28insGTGTGTTTGGGTTTTGTTGT	NP_000316.2:n.206-29_206-28insGTGTGTTTGGGTTTTGTTGT
NM_001204397.1:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	NP_001191326.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
NM_001204398.1:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	NP_001191327.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
NM_001204399.1:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	NP_001191328.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
NM_153426.2:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	NP_700475.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
NM_153427.2:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	NP_700476.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
XM_006714235.2:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	XP_006714298.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
XM_011532027.1:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	XP_011530329.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT
XM_024454090.1:c.-149-29_-149-28insGTGTGTTTGGGTTTTGTTGT	XP_024309858.1:n.-149-29_-149-28insGTGTGTTTGGGTTTTGTTGT
NM_000325.6:c.206-29_206-28insGTGTGTTTGGGTTTTGTTGT MANE Select	NP_000316.2:n.206-29_206-28insGTGTGTTTGGGTTTTGTTGT
NM_001204397.2:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	NP_001191326.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
NM_153426.3:c.185-29_185-28insGTGTGTTTGGGTTTTGTTGT	NP_700475.1:n.185-29_185-28insGTGTGTTTGGGTTTTGTTGT
NM_153427.3:c.47-29_47-28insGTGTGTTTGGGTTTTGTTGT	NP_700476.1:n.47-29_47-28insGTGTGTTTGGGTTTTGTTGT