Canonical Allele Identifier: CA104044173

Gene: PITX2

Linked Data

• dbSNP Id: rs561702585
• gnomAD v2: 4-111538758-TATAATA-T
• gnomAD v3: 4-110617602-TATAATA-T
• gnomAD v4: 4-110617602-TATAATA-T
• MyVariant Identifiers: chr4:g.111538759_111538764del (hg19) ; chr4:g.110617603_110617608del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110617612_110617617del , CM000666.2:g.110617612_110617617del	GRCh38
NC_000004.11:g.111538768_111538773del , CM000666.1:g.111538768_111538773del	GRCh37
NC_000004.10:g.111758217_111758222del	NCBI36
NG_007120.1:g.24745_24750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.*740_*745del	ENSP00000484763.2:n.*740_*745del
ENST00000614423.5:c.*517_*522del	ENSP00000481951.2:n.*517_*522del
ENST00000394595.8:c.*517_*522del	ENSP00000378095.4:n.*517_*522del
ENST00000644488.1:n.1534_1539del
ENST00000644743.1:c.*517_*522del MANE Select	ENSP00000495061.1:n.*517_*522del
ENST00000645131.1:n.1423_1428del
ENST00000306732.7:c.*517_*522del	ENSP00000304169.3:n.*517_*522del
ENST00000354925.6:c.*517_*522del	ENSP00000347004.2:n.*517_*522del
ENST00000355080.9:c.*517_*522del	ENSP00000347192.5:n.*517_*522del
ENST00000394595.7:c.*740_*745del	ENSP00000378095.3:n.*740_*745del
ENST00000394598.6:c.*517_*522del	ENSP00000378097.2:n.*517_*522del
ENST00000607868.1:n.1219_1224del
ENST00000613094.4:c.*517_*522del	ENSP00000484763.1:n.*517_*522del
ENST00000614423.4:c.*517_*522del	ENSP00000481951.1:n.*517_*522del
ENST00000616641.4:c.*517_*522del	ENSP00000484909.1:n.*517_*522del
NM_000325.5:c.*517_*522del	NP_000316.2:n.*517_*522del
NM_001204397.1:c.*517_*522del	NP_001191326.1:n.*517_*522del
NM_001204398.1:c.*517_*522del	NP_001191327.1:n.*517_*522del
NM_001204399.1:c.*517_*522del	NP_001191328.1:n.*517_*522del
NM_153426.2:c.*517_*522del	NP_700475.1:n.*517_*522del
NM_153427.2:c.*517_*522del	NP_700476.1:n.*517_*522del
XM_006714235.2:c.*517_*522del	XP_006714298.1:n.*517_*522del
XM_011532027.1:c.*517_*522del	XP_011530329.1:n.*517_*522del
XM_024454090.1:c.*517_*522del	XP_024309858.1:n.*517_*522del
NM_000325.6:c.*517_*522del MANE Select	NP_000316.2:n.*517_*522del
NM_001204397.2:c.*517_*522del	NP_001191326.1:n.*517_*522del
NM_153426.3:c.*517_*522del	NP_700475.1:n.*517_*522del
NM_153427.3:c.*517_*522del	NP_700476.1:n.*517_*522del