Canonical Allele Identifier: CA357984340

Gene: PITX2

Linked Data

• MyVariant Identifiers: chr4:g.111539772C>T (hg19) ; chr4:g.110618616C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110618616C>T , CM000666.2:g.110618616C>T	GRCh38
NC_000004.11:g.111539772C>T , CM000666.1:g.111539772C>T	GRCh37
NC_000004.10:g.111759221C>T	NCBI36
NG_007120.1:g.23737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.257G>A	ENSP00000484763.2:p.Trp86Ter
ENST00000614423.5:c.382G>A	ENSP00000481951.2:p.Gly128Ser
ENST00000616641.5:n.450G>A
ENST00000644488.2:n.454G>A
ENST00000394595.8:c.463G>A	ENSP00000378095.4:p.Gly155Ser
ENST00000644488.1:n.526G>A
ENST00000644743.1:c.484G>A MANE Select	ENSP00000495061.1:p.Gly162Ser
ENST00000645131.1:n.415G>A
ENST00000306732.7:c.484G>A	ENSP00000304169.3:p.Gly162Ser
ENST00000354925.6:c.463G>A	ENSP00000347004.2:p.Gly155Ser
ENST00000355080.9:c.325G>A	ENSP00000347192.5:p.Gly109Ser
ENST00000394595.7:c.257G>A	ENSP00000378095.3:p.Trp86Ter
ENST00000394598.6:c.463G>A	ENSP00000378097.2:p.Gly155Ser
ENST00000511837.5:c.463G>A	ENSP00000421454.1:p.Gly155Ser
ENST00000511990.1:c.325G>A	ENSP00000424142.1:p.Gly109Ser
ENST00000556049.1:n.790G>A
ENST00000607868.1:n.211G>A
ENST00000613094.4:c.463G>A	ENSP00000484763.1:p.Gly155Ser
ENST00000614423.4:c.463G>A	ENSP00000481951.1:p.Gly155Ser
ENST00000616641.4:c.325G>A	ENSP00000484909.1:p.Gly109Ser
NM_000325.5:c.484G>A	NP_000316.2:p.Gly162Ser
NM_001204397.1:c.463G>A	NP_001191326.1:p.Gly155Ser
NM_001204398.1:c.463G>A	NP_001191327.1:p.Gly155Ser
NM_001204399.1:c.325G>A	NP_001191328.1:p.Gly109Ser
NM_153426.2:c.463G>A	NP_700475.1:p.Gly155Ser
NM_153427.2:c.325G>A	NP_700476.1:p.Gly109Ser
XM_006714235.2:c.463G>A	XP_006714298.1:p.Gly155Ser
XM_011532027.1:c.325G>A	XP_011530329.1:p.Gly109Ser
XM_024454090.1:c.130G>A	XP_024309858.1:p.Gly44Ser
NM_000325.6:c.484G>A MANE Select	NP_000316.2:p.Gly162Ser
NM_001204397.2:c.463G>A	NP_001191326.1:p.Gly155Ser
NM_153426.3:c.463G>A	NP_700475.1:p.Gly155Ser
NM_153427.3:c.325G>A	NP_700476.1:p.Gly109Ser