Canonical Allele Identifier: CA446784569

Gene: PITX1

Linked Data

• dbSNP Id: rs1752444341
• gnomAD v4: 5-135031357-C-T
• MyVariant Identifiers: chr5:g.134367047C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135031357C>T , CM000667.2:g.135031357C>T	GRCh38
NC_000005.9:g.134367047C>T , CM000667.1:g.134367047C>T	GRCh37
NC_000005.8:g.134394946C>T	NCBI36
NG_012114.1:g.7918G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265340.12:c.321G>A MANE Select	ENSP00000265340.6:p.Thr107=
ENST00000265340.11:c.321G>A	ENSP00000265340.6:p.Thr107=
ENST00000502676.1:c.321G>A	ENSP00000423624.1:p.Thr107=
ENST00000503586.1:c.443G>A
ENST00000504936.1:n.654G>A
ENST00000506438.5:c.321G>A	ENSP00000427542.1:p.Thr107=
ENST00000507253.5:c.321G>A	ENSP00000422908.1:p.Thr107=
NM_002653.4:c.321G>A	NP_002644.4:p.Thr107=
NM_002653.5:c.321G>A MANE Select	NP_002644.4:p.Thr107=