Canonical Allele Identifier: CA1485098390
Gene: PITX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110618760_110618761delinsAC , CM000666.2:g.110618760_110618761delinsAC GRCh38
NC_000004.11:g.111539916_111539917delinsAC , CM000666.1:g.111539916_111539917delinsAC GRCh37
NC_000004.10:g.111759365_111759366delinsAC NCBI36
NG_007120.1:g.23592_23593delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000613094.5:c.185-73_185-72delinsGT ENSP00000484763.2:n.185-73_185-72delinsGT
ENST00000614423.5:c.310-73_310-72delinsGT ENSP00000481951.2:n.310-73_310-72delinsGT
ENST00000616641.5:n.378-73_378-72delinsGT
ENST00000644488.2:n.382-73_382-72delinsGT
ENST00000394595.8:c.391-73_391-72delinsGT ENSP00000378095.4:n.391-73_391-72delinsGT
ENST00000644488.1:n.454-73_454-72delinsGT
ENST00000644743.1:c.412-73_412-72delinsGT MANE Select ENSP00000495061.1:n.412-73_412-72delinsGT
ENST00000645131.1:n.343-73_343-72delinsGT
ENST00000306732.7:c.412-73_412-72delinsGT ENSP00000304169.3:n.412-73_412-72delinsGT
ENST00000354925.6:c.391-73_391-72delinsGT ENSP00000347004.2:n.391-73_391-72delinsGT
ENST00000355080.9:c.253-73_253-72delinsGT ENSP00000347192.5:n.253-73_253-72delinsGT
ENST00000394595.7:c.185-73_185-72delinsGT ENSP00000378095.3:n.185-73_185-72delinsGT
ENST00000394598.6:c.391-73_391-72delinsGT ENSP00000378097.2:n.391-73_391-72delinsGT
ENST00000511837.5:c.391-73_391-72delinsGT ENSP00000421454.1:n.391-73_391-72delinsGT
ENST00000511990.1:c.253-73_253-72delinsGT ENSP00000424142.1:n.253-73_253-72delinsGT
ENST00000556049.1:n.718-73_718-72delinsGT
ENST00000607868.1:n.66_67delinsGT
ENST00000613094.4:c.391-73_391-72delinsGT ENSP00000484763.1:n.391-73_391-72delinsGT
ENST00000614423.4:c.391-73_391-72delinsGT ENSP00000481951.1:n.391-73_391-72delinsGT
ENST00000616641.4:c.253-73_253-72delinsGT ENSP00000484909.1:n.253-73_253-72delinsGT
NM_000325.5:c.412-73_412-72delinsGT NP_000316.2:n.412-73_412-72delinsGT
NM_001204397.1:c.391-73_391-72delinsGT NP_001191326.1:n.391-73_391-72delinsGT
NM_001204398.1:c.391-73_391-72delinsGT NP_001191327.1:n.391-73_391-72delinsGT
NM_001204399.1:c.253-73_253-72delinsGT NP_001191328.1:n.253-73_253-72delinsGT
NM_153426.2:c.391-73_391-72delinsGT NP_700475.1:n.391-73_391-72delinsGT
NM_153427.2:c.253-73_253-72delinsGT NP_700476.1:n.253-73_253-72delinsGT
XM_006714235.2:c.391-73_391-72delinsGT XP_006714298.1:n.391-73_391-72delinsGT
XM_011532027.1:c.253-73_253-72delinsGT XP_011530329.1:n.253-73_253-72delinsGT
XM_024454090.1:c.58-73_58-72delinsGT XP_024309858.1:n.58-73_58-72delinsGT
NM_000325.6:c.412-73_412-72delinsGT MANE Select NP_000316.2:n.412-73_412-72delinsGT
NM_001204397.2:c.391-73_391-72delinsGT NP_001191326.1:n.391-73_391-72delinsGT
NM_153426.3:c.391-73_391-72delinsGT NP_700475.1:n.391-73_391-72delinsGT
NM_153427.3:c.253-73_253-72delinsGT NP_700476.1:n.253-73_253-72delinsGT