Canonical Allele Identifier: CA357984499
Gene: PITX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110618673G>A , CM000666.2:g.110618673G>A GRCh38
NC_000004.11:g.111539829G>A , CM000666.1:g.111539829G>A GRCh37
NC_000004.10:g.111759278G>A NCBI36
NG_007120.1:g.23680C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000613094.5:c.200C>T ENSP00000484763.2:p.Ser67Leu
ENST00000614423.5:c.325C>T ENSP00000481951.2:p.Arg109Cys
ENST00000616641.5:n.393C>T
ENST00000644488.2:n.397C>T
ENST00000394595.8:c.406C>T ENSP00000378095.4:p.Arg136Cys
ENST00000644488.1:n.469C>T
ENST00000644743.1:c.427C>T MANE Select ENSP00000495061.1:p.Arg143Cys
ENST00000645131.1:n.358C>T
ENST00000306732.7:c.427C>T ENSP00000304169.3:p.Arg143Cys
ENST00000354925.6:c.406C>T ENSP00000347004.2:p.Arg136Cys
ENST00000355080.9:c.268C>T ENSP00000347192.5:p.Arg90Cys
ENST00000394595.7:c.200C>T ENSP00000378095.3:p.Ser67Leu
ENST00000394598.6:c.406C>T ENSP00000378097.2:p.Arg136Cys
ENST00000511837.5:c.406C>T ENSP00000421454.1:p.Arg136Cys
ENST00000511990.1:c.268C>T ENSP00000424142.1:p.Arg90Cys
ENST00000556049.1:n.733C>T
ENST00000607868.1:n.154C>T
ENST00000613094.4:c.406C>T ENSP00000484763.1:p.Arg136Cys
ENST00000614423.4:c.406C>T ENSP00000481951.1:p.Arg136Cys
ENST00000616641.4:c.268C>T ENSP00000484909.1:p.Arg90Cys
NM_000325.5:c.427C>T NP_000316.2:p.Arg143Cys
NM_001204397.1:c.406C>T NP_001191326.1:p.Arg136Cys
NM_001204398.1:c.406C>T NP_001191327.1:p.Arg136Cys
NM_001204399.1:c.268C>T NP_001191328.1:p.Arg90Cys
NM_153426.2:c.406C>T NP_700475.1:p.Arg136Cys
NM_153427.2:c.268C>T NP_700476.1:p.Arg90Cys
XM_006714235.2:c.406C>T XP_006714298.1:p.Arg136Cys
XM_011532027.1:c.268C>T XP_011530329.1:p.Arg90Cys
XM_024454090.1:c.73C>T XP_024309858.1:p.Arg25Cys
NM_000325.6:c.427C>T MANE Select NP_000316.2:p.Arg143Cys
NM_001204397.2:c.406C>T NP_001191326.1:p.Arg136Cys
NM_153426.3:c.406C>T NP_700475.1:p.Arg136Cys
NM_153427.3:c.268C>T NP_700476.1:p.Arg90Cys