Canonical Allele Identifier: CA361028549
Gene: PITX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.134367046A>C (hg19) chr5:g.135031356A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031356A>C , CM000667.2:g.135031356A>C GRCh38
NC_000005.9:g.134367046A>C , CM000667.1:g.134367046A>C GRCh37
NC_000005.8:g.134394945A>C NCBI36
NG_012114.1:g.7919T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.322T>G MANE Select ENSP00000265340.6:p.Phe108Val
ENST00000265340.11:c.322T>G ENSP00000265340.6:p.Phe108Val
ENST00000502676.1:c.322T>G ENSP00000423624.1:p.Phe108Val
ENST00000503586.1:c.444T>G
ENST00000504936.1:n.655T>G
ENST00000506438.5:c.322T>G ENSP00000427542.1:p.Phe108Val
ENST00000507253.5:c.322T>G ENSP00000422908.1:p.Phe108Val
NM_002653.4:c.322T>G NP_002644.4:p.Phe108Val
NM_002653.5:c.322T>G MANE Select NP_002644.4:p.Phe108Val
Search 100 bp 5'
Search 100 bp 3'