Canonical Allele Identifier: CA2763074995

Gene: PITX2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110621449_110621450insACTT , CM000666.2:g.110621449_110621450insACTT	GRCh38
NC_000004.11:g.111542605_111542606insACTT , CM000666.1:g.111542605_111542606insACTT	GRCh37
NC_000004.10:g.111762054_111762055insACTT	NCBI36
NG_007120.1:g.20903_20904insAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.185-2762_185-2761insAAGT	ENSP00000484763.2:n.185-2762_185-2761insAAGT
ENST00000614423.5:c.104-81_104-80insAAGT	ENSP00000481951.2:n.104-81_104-80insAAGT
ENST00000616641.5:n.172-81_172-80insAAGT
ENST00000644488.2:n.176-81_176-80insAAGT
ENST00000394595.8:c.185-81_185-80insAAGT	ENSP00000378095.4:n.185-81_185-80insAAGT
ENST00000644488.1:n.248-81_248-80insAAGT
ENST00000644743.1:c.206-81_206-80insAAGT MANE Select	ENSP00000495061.1:n.206-81_206-80insAAGT
ENST00000645131.1:n.137-81_137-80insAAGT
ENST00000306732.7:c.206-81_206-80insAAGT	ENSP00000304169.3:n.206-81_206-80insAAGT
ENST00000354925.6:c.185-81_185-80insAAGT	ENSP00000347004.2:n.185-81_185-80insAAGT
ENST00000355080.9:c.47-81_47-80insAAGT	ENSP00000347192.5:n.47-81_47-80insAAGT
ENST00000394595.7:c.185-2762_185-2761insAAGT	ENSP00000378095.3:n.185-2762_185-2761insAAGT
ENST00000394598.6:c.185-81_185-80insAAGT	ENSP00000378097.2:n.185-81_185-80insAAGT
ENST00000511837.5:c.185-81_185-80insAAGT	ENSP00000421454.1:n.185-81_185-80insAAGT
ENST00000511990.1:c.47-81_47-80insAAGT	ENSP00000424142.1:n.47-81_47-80insAAGT
ENST00000557119.2:c.206-81_206-80insAAGT	ENSP00000475617.1:n.206-81_206-80insAAGT
ENST00000613094.4:c.185-81_185-80insAAGT	ENSP00000484763.1:n.185-81_185-80insAAGT
ENST00000614423.4:c.185-81_185-80insAAGT	ENSP00000481951.1:n.185-81_185-80insAAGT
ENST00000616641.4:c.47-81_47-80insAAGT	ENSP00000484909.1:n.47-81_47-80insAAGT
NM_000325.5:c.206-81_206-80insAAGT	NP_000316.2:n.206-81_206-80insAAGT
NM_001204397.1:c.185-81_185-80insAAGT	NP_001191326.1:n.185-81_185-80insAAGT
NM_001204398.1:c.185-81_185-80insAAGT	NP_001191327.1:n.185-81_185-80insAAGT
NM_001204399.1:c.47-81_47-80insAAGT	NP_001191328.1:n.47-81_47-80insAAGT
NM_153426.2:c.185-81_185-80insAAGT	NP_700475.1:n.185-81_185-80insAAGT
NM_153427.2:c.47-81_47-80insAAGT	NP_700476.1:n.47-81_47-80insAAGT
XM_006714235.2:c.185-81_185-80insAAGT	XP_006714298.1:n.185-81_185-80insAAGT
XM_011532027.1:c.47-81_47-80insAAGT	XP_011530329.1:n.47-81_47-80insAAGT
XM_024454090.1:c.-149-81_-149-80insAAGT	XP_024309858.1:n.-149-81_-149-80insAAGT
NM_000325.6:c.206-81_206-80insAAGT MANE Select	NP_000316.2:n.206-81_206-80insAAGT
NM_001204397.2:c.185-81_185-80insAAGT	NP_001191326.1:n.185-81_185-80insAAGT
NM_153426.3:c.185-81_185-80insAAGT	NP_700475.1:n.185-81_185-80insAAGT
NM_153427.3:c.47-81_47-80insAAGT	NP_700476.1:n.47-81_47-80insAAGT