Canonical Allele Identifier: CA1485136979

Gene: PITX2

Linked Data

• dbSNP Id: rs1728807992

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110617539G>T , CM000666.2:g.110617539G>T	GRCh38
NC_000004.11:g.111538695G>T , CM000666.1:g.111538695G>T	GRCh37
NC_000004.10:g.111758144G>T	NCBI36
NG_007120.1:g.24814C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.*809C>A	ENSP00000484763.2:n.*809C>A
ENST00000614423.5:c.*586C>A	ENSP00000481951.2:n.*586C>A
ENST00000394595.8:c.*586C>A	ENSP00000378095.4:n.*586C>A
ENST00000644488.1:n.1603C>A
ENST00000644743.1:c.*586C>A MANE Select	ENSP00000495061.1:n.*586C>A
ENST00000645131.1:n.1492C>A
ENST00000306732.7:c.*586C>A	ENSP00000304169.3:n.*586C>A
ENST00000354925.6:c.*586C>A	ENSP00000347004.2:n.*586C>A
ENST00000355080.9:c.*586C>A	ENSP00000347192.5:n.*586C>A
ENST00000394595.7:c.*809C>A	ENSP00000378095.3:n.*809C>A
ENST00000394598.6:c.*586C>A	ENSP00000378097.2:n.*586C>A
ENST00000607868.1:n.1288C>A
ENST00000613094.4:c.*586C>A	ENSP00000484763.1:n.*586C>A
ENST00000614423.4:c.*586C>A	ENSP00000481951.1:n.*586C>A
ENST00000616641.4:c.*586C>A	ENSP00000484909.1:n.*586C>A
NM_000325.5:c.*586C>A	NP_000316.2:n.*586C>A
NM_001204397.1:c.*586C>A	NP_001191326.1:n.*586C>A
NM_001204398.1:c.*586C>A	NP_001191327.1:n.*586C>A
NM_001204399.1:c.*586C>A	NP_001191328.1:n.*586C>A
NM_153426.2:c.*586C>A	NP_700475.1:n.*586C>A
NM_153427.2:c.*586C>A	NP_700476.1:n.*586C>A
XM_006714235.2:c.*586C>A	XP_006714298.1:n.*586C>A
XM_011532027.1:c.*586C>A	XP_011530329.1:n.*586C>A
XM_024454090.1:c.*586C>A	XP_024309858.1:n.*586C>A
NM_000325.6:c.*586C>A MANE Select	NP_000316.2:n.*586C>A
NM_001204397.2:c.*586C>A	NP_001191326.1:n.*586C>A
NM_153426.3:c.*586C>A	NP_700475.1:n.*586C>A
NM_153427.3:c.*586C>A	NP_700476.1:n.*586C>A