Canonical Allele Identifier: CA446784591
Gene: PITX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.134367089A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031399A>T , CM000667.2:g.135031399A>T GRCh38
NC_000005.9:g.134367089A>T , CM000667.1:g.134367089A>T GRCh37
NC_000005.8:g.134394988A>T NCBI36
NG_012114.1:g.7876T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.279T>A MANE Select ENSP00000265340.6:p.Arg93=
ENST00000265340.11:c.279T>A ENSP00000265340.6:p.Arg93=
ENST00000502676.1:c.279T>A ENSP00000423624.1:p.Arg93=
ENST00000503586.1:c.401T>A
ENST00000504936.1:n.612T>A
ENST00000506438.5:c.279T>A ENSP00000427542.1:p.Arg93=
ENST00000507253.5:c.279T>A ENSP00000422908.1:p.Arg93=
NM_002653.4:c.279T>A NP_002644.4:p.Arg93=
NM_002653.5:c.279T>A MANE Select NP_002644.4:p.Arg93=