Canonical Allele Identifier: CA1485101298

Gene: PITX2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110621216G= , CM000666.2:g.110621216G=	GRCh38
NC_000004.11:g.111542372G= , CM000666.1:g.111542372G=	GRCh37
NC_000004.10:g.111761821G=	NCBI36
NG_007120.1:g.21137C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000613094.5:c.185-2528C=	ENSP00000484763.2:n.185-2528C=
ENST00000614423.5:c.257C=	ENSP00000481951.2:p.Ser86=
ENST00000616641.5:n.325C=
ENST00000644488.2:n.329C=
ENST00000394595.8:c.338C=	ENSP00000378095.4:p.Ser113=
ENST00000644488.1:n.401C=
ENST00000644743.1:c.359C= MANE Select	ENSP00000495061.1:p.Ser120=
ENST00000645131.1:n.290C=
ENST00000306732.7:c.359C=	ENSP00000304169.3:p.Ser120=
ENST00000354925.6:c.338C=	ENSP00000347004.2:p.Ser113=
ENST00000355080.9:c.200C=	ENSP00000347192.5:p.Ser67=
ENST00000394595.7:c.185-2528C=	ENSP00000378095.3:n.185-2528C=
ENST00000394598.6:c.338C=	ENSP00000378097.2:p.Ser113=
ENST00000511837.5:c.338C=	ENSP00000421454.1:p.Ser113=
ENST00000511990.1:c.200C=	ENSP00000424142.1:p.Ser67=
ENST00000557119.2:c.359C=	ENSP00000475617.1:p.Ser120=
ENST00000613094.4:c.338C=	ENSP00000484763.1:p.Ser113=
ENST00000614423.4:c.338C=	ENSP00000481951.1:p.Ser113=
ENST00000616641.4:c.200C=	ENSP00000484909.1:p.Ser67=
NM_000325.5:c.359C=	NP_000316.2:p.Ser120=
NM_001204397.1:c.338C=	NP_001191326.1:p.Ser113=
NM_001204398.1:c.338C=	NP_001191327.1:p.Ser113=
NM_001204399.1:c.200C=	NP_001191328.1:p.Ser67=
NM_153426.2:c.338C=	NP_700475.1:p.Ser113=
NM_153427.2:c.200C=	NP_700476.1:p.Ser67=
XM_006714235.2:c.338C=	XP_006714298.1:p.Ser113=
XM_011532027.1:c.200C=	XP_011530329.1:p.Ser67=
XM_024454090.1:c.5C=	XP_024309858.1:p.Ser2=
NM_000325.6:c.359C= MANE Select	NP_000316.2:p.Ser120=
NM_001204397.2:c.338C=	NP_001191326.1:p.Ser113=
NM_153426.3:c.338C=	NP_700475.1:p.Ser113=
NM_153427.3:c.200C=	NP_700476.1:p.Ser67=