Canonical Allele Identifier: CA562836296
Gene: PITX1 HGNC NCBI

Linked Data

dbSNP Id: rs1316163217

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031859G>T , CM000667.2:g.135031859G>T GRCh38
NC_000005.9:g.134367549G>T , CM000667.1:g.134367549G>T GRCh37
NC_000005.8:g.134395448G>T NCBI36
NG_012114.1:g.7416C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.170-351C>A MANE Select ENSP00000265340.6:n.170-351C>A
ENST00000265340.11:c.170-351C>A ENSP00000265340.6:n.170-351C>A
ENST00000502676.1:c.170-351C>A ENSP00000423624.1:n.170-351C>A
ENST00000503586.1:c.292-351C>A
ENST00000504936.1:n.152C>A
ENST00000506438.5:c.170-351C>A ENSP00000427542.1:n.170-351C>A
ENST00000507253.5:c.170-351C>A ENSP00000422908.1:n.170-351C>A
NM_002653.4:c.170-351C>A NP_002644.4:n.170-351C>A
NM_002653.5:c.170-351C>A MANE Select NP_002644.4:n.170-351C>A