Canonical Allele Identifier: CA128011655

Gene: PITX1

Linked Data

• dbSNP Id: rs532815012
• gnomAD v3: 5-135031950-A-T
• gnomAD v4: 5-135031950-A-T
• MyVariant Identifiers: chr5:g.134367640A>T (hg19) ; chr5:g.135031950A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135031950A>T , CM000667.2:g.135031950A>T	GRCh38
NC_000005.9:g.134367640A>T , CM000667.1:g.134367640A>T	GRCh37
NC_000005.8:g.134395539A>T	NCBI36
NG_012114.1:g.7325T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265340.12:c.170-442T>A MANE Select	ENSP00000265340.6:n.170-442T>A
ENST00000265340.11:c.170-442T>A	ENSP00000265340.6:n.170-442T>A
ENST00000502676.1:c.170-442T>A	ENSP00000423624.1:n.170-442T>A
ENST00000503586.1:c.292-442T>A
ENST00000504936.1:n.61T>A
ENST00000506438.5:c.170-442T>A	ENSP00000427542.1:n.170-442T>A
ENST00000507253.5:c.170-442T>A	ENSP00000422908.1:n.170-442T>A
NM_002653.4:c.170-442T>A	NP_002644.4:n.170-442T>A
NM_002653.5:c.170-442T>A MANE Select	NP_002644.4:n.170-442T>A