Canonical Allele Identifier: CA357983531
Gene: PITX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110618316A>T , CM000666.2:g.110618316A>T GRCh38
NC_000004.11:g.111539472A>T , CM000666.1:g.111539472A>T GRCh37
NC_000004.10:g.111758921A>T NCBI36
NG_007120.1:g.24037T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000613094.5:c.*32T>A ENSP00000484763.2:n.*32T>A
ENST00000614423.5:c.682T>A ENSP00000481951.2:p.Ser228Thr
ENST00000616641.5:n.750T>A
ENST00000644488.2:n.754T>A
ENST00000394595.8:c.763T>A ENSP00000378095.4:p.Ser255Thr
ENST00000644488.1:n.826T>A
ENST00000644743.1:c.784T>A MANE Select ENSP00000495061.1:p.Ser262Thr
ENST00000645131.1:n.715T>A
ENST00000306732.7:c.784T>A ENSP00000304169.3:p.Ser262Thr
ENST00000354925.6:c.763T>A ENSP00000347004.2:p.Ser255Thr
ENST00000355080.9:c.625T>A ENSP00000347192.5:p.Ser209Thr
ENST00000394595.7:c.*32T>A ENSP00000378095.3:n.*32T>A
ENST00000394598.6:c.763T>A ENSP00000378097.2:p.Ser255Thr
ENST00000511837.5:c.763T>A ENSP00000421454.1:p.Ser255Thr
ENST00000607868.1:n.511T>A
ENST00000613094.4:c.763T>A ENSP00000484763.1:p.Ser255Thr
ENST00000614423.4:c.763T>A ENSP00000481951.1:p.Ser255Thr
ENST00000616641.4:c.625T>A ENSP00000484909.1:p.Ser209Thr
NM_000325.5:c.784T>A NP_000316.2:p.Ser262Thr
NM_001204397.1:c.763T>A NP_001191326.1:p.Ser255Thr
NM_001204398.1:c.763T>A NP_001191327.1:p.Ser255Thr
NM_001204399.1:c.625T>A NP_001191328.1:p.Ser209Thr
NM_153426.2:c.763T>A NP_700475.1:p.Ser255Thr
NM_153427.2:c.625T>A NP_700476.1:p.Ser209Thr
XM_006714235.2:c.763T>A XP_006714298.1:p.Ser255Thr
XM_011532027.1:c.625T>A XP_011530329.1:p.Ser209Thr
XM_024454090.1:c.430T>A XP_024309858.1:p.Ser144Thr
NM_000325.6:c.784T>A MANE Select NP_000316.2:p.Ser262Thr
NM_001204397.2:c.763T>A NP_001191326.1:p.Ser255Thr
NM_153426.3:c.763T>A NP_700475.1:p.Ser255Thr
NM_153427.3:c.625T>A NP_700476.1:p.Ser209Thr