Canonical Allele Identifier: CA104045351
Gene: PITX2 HGNC NCBI

Linked Data

dbSNP Id: rs28936408

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110622300A>T , CM000666.2:g.110622300A>T GRCh38
NC_000004.11:g.111543456A>T , CM000666.1:g.111543456A>T GRCh37
NC_000004.10:g.111762905A>T NCBI36
NG_007120.1:g.20053T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000613094.5:c.185-3612T>A ENSP00000484763.2:n.185-3612T>A
ENST00000614423.5:c.59T>A ENSP00000481951.2:p.Leu20Gln
ENST00000616641.5:n.172-931T>A
ENST00000644488.2:n.176-931T>A
ENST00000394595.8:c.185-931T>A ENSP00000378095.4:n.185-931T>A
ENST00000644488.1:n.203T>A
ENST00000644743.1:c.161T>A MANE Select ENSP00000495061.1:p.Leu54Gln
ENST00000306732.7:c.161T>A ENSP00000304169.3:p.Leu54Gln
ENST00000354925.6:c.185-931T>A ENSP00000347004.2:n.185-931T>A
ENST00000355080.9:c.47-931T>A ENSP00000347192.5:n.47-931T>A
ENST00000394595.7:c.185-3612T>A ENSP00000378095.3:n.185-3612T>A
ENST00000394598.6:c.185-931T>A ENSP00000378097.2:n.185-931T>A
ENST00000511837.5:c.185-931T>A ENSP00000421454.1:n.185-931T>A
ENST00000511990.1:c.47-931T>A ENSP00000424142.1:n.47-931T>A
ENST00000557119.2:c.161T>A ENSP00000475617.1:p.Leu54Gln
ENST00000613094.4:c.185-931T>A ENSP00000484763.1:n.185-931T>A
ENST00000614423.4:c.185-931T>A ENSP00000481951.1:n.185-931T>A
ENST00000616641.4:c.47-931T>A ENSP00000484909.1:n.47-931T>A
NM_000325.5:c.161T>A NP_000316.2:p.Leu54Gln
NM_001204397.1:c.185-931T>A NP_001191326.1:n.185-931T>A
NM_001204398.1:c.185-931T>A NP_001191327.1:n.185-931T>A
NM_001204399.1:c.47-931T>A NP_001191328.1:n.47-931T>A
NM_153426.2:c.185-931T>A NP_700475.1:n.185-931T>A
NM_153427.2:c.47-931T>A NP_700476.1:n.47-931T>A
XM_006714235.2:c.185-931T>A XP_006714298.1:n.185-931T>A
XM_011532027.1:c.47-931T>A XP_011530329.1:n.47-931T>A
NM_000325.6:c.161T>A MANE Select NP_000316.2:p.Leu54Gln
NM_001204397.2:c.185-931T>A NP_001191326.1:n.185-931T>A
NM_153426.3:c.185-931T>A NP_700475.1:n.185-931T>A
NM_153427.3:c.47-931T>A NP_700476.1:n.47-931T>A