Canonical Allele Identifier: CA785303542
Gene: PITX2 HGNC NCBI

Linked Data

dbSNP Id: rs1280192786

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110620929del , CM000666.2:g.110620929del GRCh38
NC_000004.11:g.111542085del , CM000666.1:g.111542085del GRCh37
NC_000004.10:g.111761534del NCBI36
NG_007120.1:g.21427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000613094.5:c.185-2238del ENSP00000484763.2:n.185-2238del
ENST00000614423.5:c.309+238del ENSP00000481951.2:n.309+238del
ENST00000616641.5:n.377+238del
ENST00000644488.2:n.381+238del
ENST00000394595.8:c.390+238del ENSP00000378095.4:n.390+238del
ENST00000644488.1:n.453+238del
ENST00000644743.1:c.411+238del MANE Select ENSP00000495061.1:n.411+238del
ENST00000645131.1:n.342+238del
ENST00000306732.7:c.411+238del ENSP00000304169.3:n.411+238del
ENST00000354925.6:c.390+238del ENSP00000347004.2:n.390+238del
ENST00000355080.9:c.252+238del ENSP00000347192.5:n.252+238del
ENST00000394595.7:c.185-2238del ENSP00000378095.3:n.185-2238del
ENST00000394598.6:c.390+238del ENSP00000378097.2:n.390+238del
ENST00000511837.5:c.390+238del ENSP00000421454.1:n.390+238del
ENST00000511990.1:c.252+238del ENSP00000424142.1:n.252+238del
ENST00000557119.2:c.649del ENSP00000475617.1:p.Arg217AlafsTer?
ENST00000613094.4:c.390+238del ENSP00000484763.1:n.390+238del
ENST00000614423.4:c.390+238del ENSP00000481951.1:n.390+238del
ENST00000616641.4:c.252+238del ENSP00000484909.1:n.252+238del
NM_000325.5:c.411+238del NP_000316.2:n.411+238del
NM_001204397.1:c.390+238del NP_001191326.1:n.390+238del
NM_001204398.1:c.390+238del NP_001191327.1:n.390+238del
NM_001204399.1:c.252+238del NP_001191328.1:n.252+238del
NM_153426.2:c.390+238del NP_700475.1:n.390+238del
NM_153427.2:c.252+238del NP_700476.1:n.252+238del
XM_006714235.2:c.390+238del XP_006714298.1:n.390+238del
XM_011532027.1:c.252+238del XP_011530329.1:n.252+238del
XM_024454090.1:c.57+238del XP_024309858.1:n.57+238del
NM_000325.6:c.411+238del MANE Select NP_000316.2:n.411+238del
NM_001204397.2:c.390+238del NP_001191326.1:n.390+238del
NM_153426.3:c.390+238del NP_700475.1:n.390+238del
NM_153427.3:c.252+238del NP_700476.1:n.252+238del