Canonical Allele Identifier: CA1628439716
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659761T= , CM000668.2:g.51659761T= GRCh38
NC_000006.11:g.51524559T= , CM000668.1:g.51524559T= GRCh37
NC_000006.10:g.51632518T= NCBI36
NG_008753.1:g.432865A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.10365A= MANE Select ENSP00000360158.3:p.Ser3455=
ENST00000371117.7:c.10365A= ENSP00000360158.3:p.Ser3455=
NM_138694.3:c.10365A= NP_619639.3:p.Ser3455=
XM_011514679.1:c.10365A= XP_011512981.1:p.Ser3455=
XM_011514680.1:c.10365A= XP_011512982.1:p.Ser3455=
XM_011514681.1:c.10236A= XP_011512983.1:p.Ser3412=
XM_011514682.1:c.10227A= XP_011512984.1:p.Ser3409=
XM_011514683.1:c.9723A= XP_011512985.1:p.Ser3241=
XM_011514684.1:c.9654A= XP_011512986.1:p.Ser3218=
XM_011514687.1:c.10157-10541A= XP_011512989.1:n.10157-10541A=
XM_011514690.1:c.4440A= XP_011512992.1:p.Ser1480=
XM_011514691.1:c.4440A= XP_011512993.1:p.Ser1480=
XR_926870.1:n.535+7388T=
XR_926871.1:n.403+7388T=
XR_926872.1:n.535+7388T=
XM_011514680.3:c.10365A= XP_011512982.1:p.Ser3455=
XM_011514682.3:c.10227A= XP_011512984.1:p.Ser3409=
XM_011514683.3:c.9723A= XP_011512985.1:p.Ser3241=
XM_011514684.3:c.9654A= XP_011512986.1:p.Ser3218=
XM_011514690.3:c.4440A= XP_011512992.1:p.Ser1480=
XM_011514691.3:c.4440A= XP_011512993.1:p.Ser1480=
XM_017010944.2:c.10365A= XP_016866433.1:p.Ser3455=
XM_017010945.2:c.10290A= XP_016866434.1:p.Ser3430=
XM_017010946.2:c.10170A= XP_016866435.1:p.Ser3390=
XM_017010947.2:c.10101A= XP_016866436.1:p.Ser3367=
XM_017010948.2:c.9654A= XP_016866437.1:p.Ser3218=
XM_017010949.2:c.8505A= XP_016866438.1:p.Ser2835=
XR_001743469.1:n.10641A=
XR_001744157.1:n.3145+7388T=
XR_926870.2:n.3145+7388T=
XR_926871.2:n.3013+7388T=
XR_926872.2:n.3145+7388T=
NM_138694.4:c.10365A= MANE Select NP_619639.3:p.Ser3455=