Canonical Allele Identifier: CA2763074900
Gene: PITX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110621371_110621372insAGTA , CM000666.2:g.110621371_110621372insAGTA GRCh38
NC_000004.11:g.111542527_111542528insAGTA , CM000666.1:g.111542527_111542528insAGTA GRCh37
NC_000004.10:g.111761976_111761977insAGTA NCBI36
NG_007120.1:g.20981_20982insTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000613094.5:c.185-2684_185-2683insTACT ENSP00000484763.2:n.185-2684_185-2683insTACT
ENST00000614423.5:c.104-3_104-2insTACT ENSP00000481951.2:n.104-3_104-2insTACT
ENST00000616641.5:n.172-3_172-2insTACT
ENST00000644488.2:n.176-3_176-2insTACT
ENST00000394595.8:c.185-3_185-2insTACT ENSP00000378095.4:n.185-3_185-2insTACT
ENST00000644488.1:n.248-3_248-2insTACT
ENST00000644743.1:c.206-3_206-2insTACT MANE Select ENSP00000495061.1:n.206-3_206-2insTACT
ENST00000645131.1:n.137-3_137-2insTACT
ENST00000306732.7:c.206-3_206-2insTACT ENSP00000304169.3:n.206-3_206-2insTACT
ENST00000354925.6:c.185-3_185-2insTACT ENSP00000347004.2:n.185-3_185-2insTACT
ENST00000355080.9:c.47-3_47-2insTACT ENSP00000347192.5:n.47-3_47-2insTACT
ENST00000394595.7:c.185-2684_185-2683insTACT ENSP00000378095.3:n.185-2684_185-2683insTACT
ENST00000394598.6:c.185-3_185-2insTACT ENSP00000378097.2:n.185-3_185-2insTACT
ENST00000511837.5:c.185-3_185-2insTACT ENSP00000421454.1:n.185-3_185-2insTACT
ENST00000511990.1:c.47-3_47-2insTACT ENSP00000424142.1:n.47-3_47-2insTACT
ENST00000557119.2:c.206-3_206-2insTACT ENSP00000475617.1:n.206-3_206-2insTACT
ENST00000613094.4:c.185-3_185-2insTACT ENSP00000484763.1:n.185-3_185-2insTACT
ENST00000614423.4:c.185-3_185-2insTACT ENSP00000481951.1:n.185-3_185-2insTACT
ENST00000616641.4:c.47-3_47-2insTACT ENSP00000484909.1:n.47-3_47-2insTACT
NM_000325.5:c.206-3_206-2insTACT NP_000316.2:n.206-3_206-2insTACT
NM_001204397.1:c.185-3_185-2insTACT NP_001191326.1:n.185-3_185-2insTACT
NM_001204398.1:c.185-3_185-2insTACT NP_001191327.1:n.185-3_185-2insTACT
NM_001204399.1:c.47-3_47-2insTACT NP_001191328.1:n.47-3_47-2insTACT
NM_153426.2:c.185-3_185-2insTACT NP_700475.1:n.185-3_185-2insTACT
NM_153427.2:c.47-3_47-2insTACT NP_700476.1:n.47-3_47-2insTACT
XM_006714235.2:c.185-3_185-2insTACT XP_006714298.1:n.185-3_185-2insTACT
XM_011532027.1:c.47-3_47-2insTACT XP_011530329.1:n.47-3_47-2insTACT
XM_024454090.1:c.-149-3_-149-2insTACT XP_024309858.1:n.-149-3_-149-2insTACT
NM_000325.6:c.206-3_206-2insTACT MANE Select NP_000316.2:n.206-3_206-2insTACT
NM_001204397.2:c.185-3_185-2insTACT NP_001191326.1:n.185-3_185-2insTACT
NM_153426.3:c.185-3_185-2insTACT NP_700475.1:n.185-3_185-2insTACT
NM_153427.3:c.47-3_47-2insTACT NP_700476.1:n.47-3_47-2insTACT