Canonical Allele Identifier: CA7914897

Gene: PDXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15008813C>A , CM000678.2:g.15008813C>A	GRCh38
NC_000016.9:g.15102670C>A , CM000678.1:g.15102670C>A	GRCh37
NC_000016.8:g.15010171C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396410.9:c.614C>A MANE Select	ENSP00000379691.4:p.Pro205His
ENST00000325823.11:c.614C>A	ENSP00000322807.8:p.Pro205His
ENST00000396410.8:c.614C>A	ENSP00000379691.4:p.Pro205His
ENST00000450288.3:c.341C>A	ENSP00000391147.3:p.Pro114His
ENST00000455313.6:c.580-868C>A	ENSP00000406703.2:n.580-868C>A
ENST00000535621.6:c.614C>A	ENSP00000437835.2:p.Pro205His
ENST00000562119.5:c.174+7025C>A	ENSP00000455486.1:n.174+7025C>A
ENST00000563679.5:c.668C>A	ENSP00000454791.1:p.Pro223His
ENST00000565362.5:c.*399C>A	ENSP00000454279.1:n.*399C>A
ENST00000567306.5:c.535-868C>A	ENSP00000454910.1:n.535-868C>A
ENST00000569715.5:c.533C>A	ENSP00000455070.1:p.Pro178His
ENST00000570001.5:n.709C>A
ENST00000627450.2:c.530C>A	ENSP00000486662.1:p.Pro177His
NM_001285444.1:c.533C>A	NP_001272373.1:p.Pro178His
NM_001285445.1:c.530C>A	NP_001272374.1:p.Pro177His
NM_001285447.1:c.569C>A	NP_001272376.1:p.Pro190His
NM_001285448.1:c.341C>A	NP_001272377.1:p.Pro114His
NM_001285449.1:c.614C>A	NP_001272378.1:p.Pro205His
NM_001285450.1:c.580-868C>A	NP_001272379.1:n.580-868C>A
NM_015027.3:c.614C>A	NP_055842.2:p.Pro205His
XM_005255173.1:c.668C>A	XP_005255230.1:p.Pro223His
XM_005255176.2:c.569C>A	XP_005255233.1:p.Pro190His
XM_006720865.2:c.488C>A	XP_006720928.2:p.Pro163His
XM_011522428.1:c.668C>A	XP_011520730.1:p.Pro223His
NM_001324019.1:c.611C>A	NP_001310948.1:p.Pro204His
NM_001324020.1:c.611C>A	NP_001310949.1:p.Pro204His
NM_001324021.1:c.533C>A	NP_001310950.1:p.Pro178His
XM_005255176.3:c.569C>A	XP_005255233.1:p.Pro190His
XM_017023059.1:c.569C>A	XP_016878548.1:p.Pro190His
XM_017023060.1:c.641C>A	XP_016878549.1:p.Pro214His
XM_017023061.2:c.569C>A	XP_016878550.1:p.Pro190His
XM_017023062.1:c.569C>A	XP_016878551.1:p.Pro190His
XM_017023063.1:c.569C>A	XP_016878552.1:p.Pro190His
XM_017023064.1:c.488C>A	XP_016878553.1:p.Pro163His
XM_017023065.1:c.569C>A	XP_016878554.1:p.Pro190His
XM_024450194.1:c.569C>A	XP_024305962.1:p.Pro190His
XM_024450195.1:c.668C>A	XP_024305963.1:p.Pro223His
XM_024450196.1:c.641C>A	XP_024305964.1:p.Pro214His
XM_024450197.1:c.488C>A	XP_024305965.1:p.Pro163His
NM_001285444.2:c.533C>A	NP_001272373.1:p.Pro178His
NM_001285445.2:c.530C>A	NP_001272374.1:p.Pro177His
NM_001285450.2:c.580-868C>A	NP_001272379.1:n.580-868C>A
NM_001324019.2:c.611C>A	NP_001310948.1:p.Pro204His
NM_015027.4:c.614C>A MANE Select	NP_055842.2:p.Pro205His
NM_001285449.2:c.614C>A	NP_001272378.1:p.Pro205His
NM_001324020.2:c.611C>A	NP_001310949.1:p.Pro204His
NM_001324021.2:c.533C>A	NP_001310950.1:p.Pro178His