Canonical Allele Identifier: CA1485098216
Gene: PITX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110618620C= , CM000666.2:g.110618620C= GRCh38
NC_000004.11:g.111539776C= , CM000666.1:g.111539776C= GRCh37
NC_000004.10:g.111759225C= NCBI36
NG_007120.1:g.23733G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000613094.5:c.253G= ENSP00000484763.2:p.Glu85=
ENST00000614423.5:c.378G= ENSP00000481951.2:p.Lys126=
ENST00000616641.5:n.446G=
ENST00000644488.2:n.450G=
ENST00000394595.8:c.459G= ENSP00000378095.4:p.Lys153=
ENST00000644488.1:n.522G=
ENST00000644743.1:c.480G= MANE Select ENSP00000495061.1:p.Lys160=
ENST00000645131.1:n.411G=
ENST00000306732.7:c.480G= ENSP00000304169.3:p.Lys160=
ENST00000354925.6:c.459G= ENSP00000347004.2:p.Lys153=
ENST00000355080.9:c.321G= ENSP00000347192.5:p.Lys107=
ENST00000394595.7:c.253G= ENSP00000378095.3:p.Glu85=
ENST00000394598.6:c.459G= ENSP00000378097.2:p.Lys153=
ENST00000511837.5:c.459G= ENSP00000421454.1:p.Lys153=
ENST00000511990.1:c.321G= ENSP00000424142.1:p.Lys107=
ENST00000556049.1:n.786G=
ENST00000607868.1:n.207G=
ENST00000613094.4:c.459G= ENSP00000484763.1:p.Lys153=
ENST00000614423.4:c.459G= ENSP00000481951.1:p.Lys153=
ENST00000616641.4:c.321G= ENSP00000484909.1:p.Lys107=
NM_000325.5:c.480G= NP_000316.2:p.Lys160=
NM_001204397.1:c.459G= NP_001191326.1:p.Lys153=
NM_001204398.1:c.459G= NP_001191327.1:p.Lys153=
NM_001204399.1:c.321G= NP_001191328.1:p.Lys107=
NM_153426.2:c.459G= NP_700475.1:p.Lys153=
NM_153427.2:c.321G= NP_700476.1:p.Lys107=
XM_006714235.2:c.459G= XP_006714298.1:p.Lys153=
XM_011532027.1:c.321G= XP_011530329.1:p.Lys107=
XM_024454090.1:c.126G= XP_024309858.1:p.Lys42=
NM_000325.6:c.480G= MANE Select NP_000316.2:p.Lys160=
NM_001204397.2:c.459G= NP_001191326.1:p.Lys153=
NM_153426.3:c.459G= NP_700475.1:p.Lys153=
NM_153427.3:c.321G= NP_700476.1:p.Lys107=