Canonical Allele Identifier: CA128010820
Gene: PITX1 HGNC NCBI

Linked Data

dbSNP Id: rs780976853
gnomAD v2: 5-134366737-G-T
gnomAD v3: 5-135031047-G-T
gnomAD v4: 5-135031047-G-T
MyVariant Identifiers: chr5:g.134366737G>T (hg19) chr5:g.135031047G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135031047G>T , CM000667.2:g.135031047G>T GRCh38
NC_000005.9:g.134366737G>T , CM000667.1:g.134366737G>T GRCh37
NC_000005.8:g.134394636G>T NCBI36
NG_012114.1:g.8228C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265340.12:c.402+229C>A MANE Select ENSP00000265340.6:n.402+229C>A
ENST00000265340.11:c.402+229C>A ENSP00000265340.6:n.402+229C>A
ENST00000503586.1:c.524+229C>A
ENST00000504936.1:n.735+229C>A
ENST00000506438.5:c.402+229C>A ENSP00000427542.1:n.402+229C>A
NM_002653.4:c.402+229C>A NP_002644.4:n.402+229C>A
NM_002653.5:c.402+229C>A MANE Select NP_002644.4:n.402+229C>A
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