Canonical Allele Identifier: CA553984548

Gene: PITX2

Linked Data

• dbSNP Id: rs1307186418
• gnomAD v2: 4-111539941-G-GCTAGCGCACTCACACACC
• gnomAD v4: 4-110618785-G-GCTAGCGCACTCACACACC
• MyVariant Identifiers: chr4:g.111539941_111539942insCTAGCGCACTCACACACC (hg19) ; chr4:g.110618785_110618786insCTAGCGCACTCACACACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110618788_110618805dup , CM000666.2:g.110618788_110618805dup	GRCh38
NC_000004.11:g.111539944_111539961dup , CM000666.1:g.111539944_111539961dup	GRCh37
NC_000004.10:g.111759393_111759410dup	NCBI36
NG_007120.1:g.23550_23567dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.185-115_185-98dup	ENSP00000484763.2:n.185-115_185-98dup
ENST00000614423.5:c.310-115_310-98dup	ENSP00000481951.2:n.310-115_310-98dup
ENST00000616641.5:n.378-115_378-98dup
ENST00000644488.2:n.382-115_382-98dup
ENST00000394595.8:c.391-115_391-98dup	ENSP00000378095.4:n.391-115_391-98dup
ENST00000644488.1:n.454-115_454-98dup
ENST00000644743.1:c.412-115_412-98dup MANE Select	ENSP00000495061.1:n.412-115_412-98dup
ENST00000645131.1:n.343-115_343-98dup
ENST00000306732.7:c.412-115_412-98dup	ENSP00000304169.3:n.412-115_412-98dup
ENST00000354925.6:c.391-115_391-98dup	ENSP00000347004.2:n.391-115_391-98dup
ENST00000355080.9:c.253-115_253-98dup	ENSP00000347192.5:n.253-115_253-98dup
ENST00000394595.7:c.185-115_185-98dup	ENSP00000378095.3:n.185-115_185-98dup
ENST00000394598.6:c.391-115_391-98dup	ENSP00000378097.2:n.391-115_391-98dup
ENST00000511837.5:c.391-115_391-98dup	ENSP00000421454.1:n.391-115_391-98dup
ENST00000511990.1:c.253-115_253-98dup	ENSP00000424142.1:n.253-115_253-98dup
ENST00000556049.1:n.718-115_718-98dup
ENST00000607868.1:n.24_41dup
ENST00000613094.4:c.391-115_391-98dup	ENSP00000484763.1:n.391-115_391-98dup
ENST00000614423.4:c.391-115_391-98dup	ENSP00000481951.1:n.391-115_391-98dup
ENST00000616641.4:c.253-115_253-98dup	ENSP00000484909.1:n.253-115_253-98dup
NM_000325.5:c.412-115_412-98dup	NP_000316.2:n.412-115_412-98dup
NM_001204397.1:c.391-115_391-98dup	NP_001191326.1:n.391-115_391-98dup
NM_001204398.1:c.391-115_391-98dup	NP_001191327.1:n.391-115_391-98dup
NM_001204399.1:c.253-115_253-98dup	NP_001191328.1:n.253-115_253-98dup
NM_153426.2:c.391-115_391-98dup	NP_700475.1:n.391-115_391-98dup
NM_153427.2:c.253-115_253-98dup	NP_700476.1:n.253-115_253-98dup
XM_006714235.2:c.391-115_391-98dup	XP_006714298.1:n.391-115_391-98dup
XM_011532027.1:c.253-115_253-98dup	XP_011530329.1:n.253-115_253-98dup
XM_024454090.1:c.58-115_58-98dup	XP_024309858.1:n.58-115_58-98dup
NM_000325.6:c.412-115_412-98dup MANE Select	NP_000316.2:n.412-115_412-98dup
NM_001204397.2:c.391-115_391-98dup	NP_001191326.1:n.391-115_391-98dup
NM_153426.3:c.391-115_391-98dup	NP_700475.1:n.391-115_391-98dup
NM_153427.3:c.253-115_253-98dup	NP_700476.1:n.253-115_253-98dup