Canonical Allele Identifier: CA357985629

Gene: PITX2

Linked Data

• MyVariant Identifiers: chr4:g.111542439G>C (hg19) ; chr4:g.110621283G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110621283G>C , CM000666.2:g.110621283G>C	GRCh38
NC_000004.11:g.111542439G>C , CM000666.1:g.111542439G>C	GRCh37
NC_000004.10:g.111761888G>C	NCBI36
NG_007120.1:g.21070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.185-2595C>G	ENSP00000484763.2:n.185-2595C>G
ENST00000614423.5:c.190C>G	ENSP00000481951.2:p.His64Asp
ENST00000616641.5:n.258C>G
ENST00000644488.2:n.262C>G
ENST00000394595.8:c.271C>G	ENSP00000378095.4:p.His91Asp
ENST00000644488.1:n.334C>G
ENST00000644743.1:c.292C>G MANE Select	ENSP00000495061.1:p.His98Asp
ENST00000645131.1:n.223C>G
ENST00000306732.7:c.292C>G	ENSP00000304169.3:p.His98Asp
ENST00000354925.6:c.271C>G	ENSP00000347004.2:p.His91Asp
ENST00000355080.9:c.133C>G	ENSP00000347192.5:p.His45Asp
ENST00000394595.7:c.185-2595C>G	ENSP00000378095.3:n.185-2595C>G
ENST00000394598.6:c.271C>G	ENSP00000378097.2:p.His91Asp
ENST00000511837.5:c.271C>G	ENSP00000421454.1:p.His91Asp
ENST00000511990.1:c.133C>G	ENSP00000424142.1:p.His45Asp
ENST00000557119.2:c.292C>G	ENSP00000475617.1:p.His98Asp
ENST00000613094.4:c.271C>G	ENSP00000484763.1:p.His91Asp
ENST00000614423.4:c.271C>G	ENSP00000481951.1:p.His91Asp
ENST00000616641.4:c.133C>G	ENSP00000484909.1:p.His45Asp
NM_000325.5:c.292C>G	NP_000316.2:p.His98Asp
NM_001204397.1:c.271C>G	NP_001191326.1:p.His91Asp
NM_001204398.1:c.271C>G	NP_001191327.1:p.His91Asp
NM_001204399.1:c.133C>G	NP_001191328.1:p.His45Asp
NM_153426.2:c.271C>G	NP_700475.1:p.His91Asp
NM_153427.2:c.133C>G	NP_700476.1:p.His45Asp
XM_006714235.2:c.271C>G	XP_006714298.1:p.His91Asp
XM_011532027.1:c.133C>G	XP_011530329.1:p.His45Asp
XM_024454090.1:c.-63C>G	XP_024309858.1:n.-63C>G
NM_000325.6:c.292C>G MANE Select	NP_000316.2:p.His98Asp
NM_001204397.2:c.271C>G	NP_001191326.1:p.His91Asp
NM_153426.3:c.271C>G	NP_700475.1:p.His91Asp
NM_153427.3:c.133C>G	NP_700476.1:p.His45Asp