Canonical Allele Identifier: CA1485137022

Gene: PITX2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110617633G= , CM000666.2:g.110617633G=	GRCh38
NC_000004.11:g.111538789G= , CM000666.1:g.111538789G=	GRCh37
NC_000004.10:g.111758238G=	NCBI36
NG_007120.1:g.24720C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.*715C=	ENSP00000484763.2:n.*715C=
ENST00000614423.5:c.*492C=	ENSP00000481951.2:n.*492C=
ENST00000394595.8:c.*492C=	ENSP00000378095.4:n.*492C=
ENST00000644488.1:n.1509C=
ENST00000644743.1:c.*492C= MANE Select	ENSP00000495061.1:n.*492C=
ENST00000645131.1:n.1398C=
ENST00000306732.7:c.*492C=	ENSP00000304169.3:n.*492C=
ENST00000354925.6:c.*492C=	ENSP00000347004.2:n.*492C=
ENST00000355080.9:c.*492C=	ENSP00000347192.5:n.*492C=
ENST00000394595.7:c.*715C=	ENSP00000378095.3:n.*715C=
ENST00000394598.6:c.*492C=	ENSP00000378097.2:n.*492C=
ENST00000607868.1:n.1194C=
ENST00000613094.4:c.*492C=	ENSP00000484763.1:n.*492C=
ENST00000614423.4:c.*492C=	ENSP00000481951.1:n.*492C=
ENST00000616641.4:c.*492C=	ENSP00000484909.1:n.*492C=
NM_000325.5:c.*492C=	NP_000316.2:n.*492C=
NM_001204397.1:c.*492C=	NP_001191326.1:n.*492C=
NM_001204398.1:c.*492C=	NP_001191327.1:n.*492C=
NM_001204399.1:c.*492C=	NP_001191328.1:n.*492C=
NM_153426.2:c.*492C=	NP_700475.1:n.*492C=
NM_153427.2:c.*492C=	NP_700476.1:n.*492C=
XM_006714235.2:c.*492C=	XP_006714298.1:n.*492C=
XM_011532027.1:c.*492C=	XP_011530329.1:n.*492C=
XM_024454090.1:c.*492C=	XP_024309858.1:n.*492C=
NM_000325.6:c.*492C= MANE Select	NP_000316.2:n.*492C=
NM_001204397.2:c.*492C=	NP_001191326.1:n.*492C=
NM_153426.3:c.*492C=	NP_700475.1:n.*492C=
NM_153427.3:c.*492C=	NP_700476.1:n.*492C=