Canonical Allele Identifier: CA446784555
Gene: PITX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.134367023G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031333G>A , CM000667.2:g.135031333G>A GRCh38
NC_000005.9:g.134367023G>A , CM000667.1:g.134367023G>A GRCh37
NC_000005.8:g.134394922G>A NCBI36
NG_012114.1:g.7942C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.345C>T MANE Select ENSP00000265340.6:p.Asp115=
ENST00000265340.11:c.345C>T ENSP00000265340.6:p.Asp115=
ENST00000503586.1:c.467C>T
ENST00000504936.1:n.678C>T
ENST00000506438.5:c.345C>T ENSP00000427542.1:p.Asp115=
ENST00000507253.5:c.345C>T ENSP00000422908.1:p.Asp115=
NM_002653.4:c.345C>T NP_002644.4:p.Asp115=
NM_002653.5:c.345C>T MANE Select NP_002644.4:p.Asp115=