Canonical Allele Identifier: CA16044258
Gene: PITX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 375437
ClinVar RCV Id: RCV000416527
dbSNP Id: rs1057519484

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110621225G>A , CM000666.2:g.110621225G>A GRCh38
NC_000004.11:g.111542381G>A , CM000666.1:g.111542381G>A GRCh37
NC_000004.10:g.111761830G>A NCBI36
NG_007120.1:g.21128C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000613094.5:c.185-2537C>T ENSP00000484763.2:n.185-2537C>T
ENST00000614423.5:c.248C>T ENSP00000481951.2:p.Pro83Leu
ENST00000616641.5:n.316C>T
ENST00000644488.2:n.320C>T
ENST00000394595.8:c.329C>T ENSP00000378095.4:p.Pro110Leu
ENST00000644488.1:n.392C>T
ENST00000644743.1:c.350C>T MANE Select ENSP00000495061.1:p.Pro117Leu
ENST00000645131.1:n.281C>T
ENST00000306732.7:c.350C>T ENSP00000304169.3:p.Pro117Leu
ENST00000354925.6:c.329C>T ENSP00000347004.2:p.Pro110Leu
ENST00000355080.9:c.191C>T ENSP00000347192.5:p.Pro64Leu
ENST00000394595.7:c.185-2537C>T ENSP00000378095.3:n.185-2537C>T
ENST00000394598.6:c.329C>T ENSP00000378097.2:p.Pro110Leu
ENST00000511837.5:c.329C>T ENSP00000421454.1:p.Pro110Leu
ENST00000511990.1:c.191C>T ENSP00000424142.1:p.Pro64Leu
ENST00000557119.2:c.350C>T ENSP00000475617.1:p.Pro117Leu
ENST00000613094.4:c.329C>T ENSP00000484763.1:p.Pro110Leu
ENST00000614423.4:c.329C>T ENSP00000481951.1:p.Pro110Leu
ENST00000616641.4:c.191C>T ENSP00000484909.1:p.Pro64Leu
NM_000325.5:c.350C>T NP_000316.2:p.Pro117Leu
NM_001204397.1:c.329C>T NP_001191326.1:p.Pro110Leu
NM_001204398.1:c.329C>T NP_001191327.1:p.Pro110Leu
NM_001204399.1:c.191C>T NP_001191328.1:p.Pro64Leu
NM_153426.2:c.329C>T NP_700475.1:p.Pro110Leu
NM_153427.2:c.191C>T NP_700476.1:p.Pro64Leu
XM_006714235.2:c.329C>T XP_006714298.1:p.Pro110Leu
XM_011532027.1:c.191C>T XP_011530329.1:p.Pro64Leu
XM_024454090.1:c.-5C>T XP_024309858.1:n.-5C>T
NM_000325.6:c.350C>T MANE Select NP_000316.2:p.Pro117Leu
NM_001204397.2:c.329C>T NP_001191326.1:p.Pro110Leu
NM_153426.3:c.329C>T NP_700475.1:p.Pro110Leu
NM_153427.3:c.191C>T NP_700476.1:p.Pro64Leu