Canonical Allele Identifier: CA1628439405
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659624T= , CM000668.2:g.51659624T= GRCh38
NC_000006.11:g.51524422T= , CM000668.1:g.51524422T= GRCh37
NC_000006.10:g.51632381T= NCBI36
NG_008753.1:g.433002A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.10502A= MANE Select ENSP00000360158.3:p.His3501=
ENST00000371117.7:c.10502A= ENSP00000360158.3:p.His3501=
NM_138694.3:c.10502A= NP_619639.3:p.His3501=
XM_011514679.1:c.10502A= XP_011512981.1:p.His3501=
XM_011514680.1:c.10502A= XP_011512982.1:p.His3501=
XM_011514681.1:c.10373A= XP_011512983.1:p.His3458=
XM_011514682.1:c.10364A= XP_011512984.1:p.His3455=
XM_011514683.1:c.9860A= XP_011512985.1:p.His3287=
XM_011514684.1:c.9791A= XP_011512986.1:p.His3264=
XM_011514687.1:c.10157-10404A= XP_011512989.1:n.10157-10404A=
XM_011514690.1:c.4577A= XP_011512992.1:p.His1526=
XM_011514691.1:c.4577A= XP_011512993.1:p.His1526=
XR_926870.1:n.535+7251T=
XR_926871.1:n.403+7251T=
XR_926872.1:n.535+7251T=
XM_011514680.3:c.10502A= XP_011512982.1:p.His3501=
XM_011514682.3:c.10364A= XP_011512984.1:p.His3455=
XM_011514683.3:c.9860A= XP_011512985.1:p.His3287=
XM_011514684.3:c.9791A= XP_011512986.1:p.His3264=
XM_011514690.3:c.4577A= XP_011512992.1:p.His1526=
XM_011514691.3:c.4577A= XP_011512993.1:p.His1526=
XM_017010944.2:c.10502A= XP_016866433.1:p.His3501=
XM_017010945.2:c.10427A= XP_016866434.1:p.His3476=
XM_017010946.2:c.10307A= XP_016866435.1:p.His3436=
XM_017010947.2:c.10238A= XP_016866436.1:p.His3413=
XM_017010948.2:c.9791A= XP_016866437.1:p.His3264=
XM_017010949.2:c.8642A= XP_016866438.1:p.His2881=
XR_001743469.1:n.10778A=
XR_001744157.1:n.3145+7251T=
XR_926870.2:n.3145+7251T=
XR_926871.2:n.3013+7251T=
XR_926872.2:n.3145+7251T=
NM_138694.4:c.10502A= MANE Select NP_619639.3:p.His3501=