Canonical Allele Identifier: CA1628439400
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659621T= , CM000668.2:g.51659621T= GRCh38
NC_000006.11:g.51524419T= , CM000668.1:g.51524419T= GRCh37
NC_000006.10:g.51632378T= NCBI36
NG_008753.1:g.433005A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.10505A= MANE Select ENSP00000360158.3:p.Glu3502=
ENST00000371117.7:c.10505A= ENSP00000360158.3:p.Glu3502=
NM_138694.3:c.10505A= NP_619639.3:p.Glu3502=
XM_011514679.1:c.10505A= XP_011512981.1:p.Glu3502=
XM_011514680.1:c.10505A= XP_011512982.1:p.Glu3502=
XM_011514681.1:c.10376A= XP_011512983.1:p.Glu3459=
XM_011514682.1:c.10367A= XP_011512984.1:p.Glu3456=
XM_011514683.1:c.9863A= XP_011512985.1:p.Glu3288=
XM_011514684.1:c.9794A= XP_011512986.1:p.Glu3265=
XM_011514687.1:c.10157-10401A= XP_011512989.1:n.10157-10401A=
XM_011514690.1:c.4580A= XP_011512992.1:p.Glu1527=
XM_011514691.1:c.4580A= XP_011512993.1:p.Glu1527=
XR_926870.1:n.535+7248T=
XR_926871.1:n.403+7248T=
XR_926872.1:n.535+7248T=
XM_011514680.3:c.10505A= XP_011512982.1:p.Glu3502=
XM_011514682.3:c.10367A= XP_011512984.1:p.Glu3456=
XM_011514683.3:c.9863A= XP_011512985.1:p.Glu3288=
XM_011514684.3:c.9794A= XP_011512986.1:p.Glu3265=
XM_011514690.3:c.4580A= XP_011512992.1:p.Glu1527=
XM_011514691.3:c.4580A= XP_011512993.1:p.Glu1527=
XM_017010944.2:c.10505A= XP_016866433.1:p.Glu3502=
XM_017010945.2:c.10430A= XP_016866434.1:p.Glu3477=
XM_017010946.2:c.10310A= XP_016866435.1:p.Glu3437=
XM_017010947.2:c.10241A= XP_016866436.1:p.Glu3414=
XM_017010948.2:c.9794A= XP_016866437.1:p.Glu3265=
XM_017010949.2:c.8645A= XP_016866438.1:p.Glu2882=
XR_001743469.1:n.10781A=
XR_001744157.1:n.3145+7248T=
XR_926870.2:n.3145+7248T=
XR_926871.2:n.3013+7248T=
XR_926872.2:n.3145+7248T=
NM_138694.4:c.10505A= MANE Select NP_619639.3:p.Glu3502=