Canonical Allele Identifier: CA1628439408
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659626G= , CM000668.2:g.51659626G= GRCh38
NC_000006.11:g.51524424G= , CM000668.1:g.51524424G= GRCh37
NC_000006.10:g.51632383G= NCBI36
NG_008753.1:g.433000C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.10500C= MANE Select ENSP00000360158.3:p.Tyr3500=
ENST00000371117.7:c.10500C= ENSP00000360158.3:p.Tyr3500=
NM_138694.3:c.10500C= NP_619639.3:p.Tyr3500=
XM_011514679.1:c.10500C= XP_011512981.1:p.Tyr3500=
XM_011514680.1:c.10500C= XP_011512982.1:p.Tyr3500=
XM_011514681.1:c.10371C= XP_011512983.1:p.Tyr3457=
XM_011514682.1:c.10362C= XP_011512984.1:p.Tyr3454=
XM_011514683.1:c.9858C= XP_011512985.1:p.Tyr3286=
XM_011514684.1:c.9789C= XP_011512986.1:p.Tyr3263=
XM_011514687.1:c.10157-10406C= XP_011512989.1:n.10157-10406C=
XM_011514690.1:c.4575C= XP_011512992.1:p.Tyr1525=
XM_011514691.1:c.4575C= XP_011512993.1:p.Tyr1525=
XR_926870.1:n.535+7253G=
XR_926871.1:n.403+7253G=
XR_926872.1:n.535+7253G=
XM_011514680.3:c.10500C= XP_011512982.1:p.Tyr3500=
XM_011514682.3:c.10362C= XP_011512984.1:p.Tyr3454=
XM_011514683.3:c.9858C= XP_011512985.1:p.Tyr3286=
XM_011514684.3:c.9789C= XP_011512986.1:p.Tyr3263=
XM_011514690.3:c.4575C= XP_011512992.1:p.Tyr1525=
XM_011514691.3:c.4575C= XP_011512993.1:p.Tyr1525=
XM_017010944.2:c.10500C= XP_016866433.1:p.Tyr3500=
XM_017010945.2:c.10425C= XP_016866434.1:p.Tyr3475=
XM_017010946.2:c.10305C= XP_016866435.1:p.Tyr3435=
XM_017010947.2:c.10236C= XP_016866436.1:p.Tyr3412=
XM_017010948.2:c.9789C= XP_016866437.1:p.Tyr3263=
XM_017010949.2:c.8640C= XP_016866438.1:p.Tyr2880=
XR_001743469.1:n.10776C=
XR_001744157.1:n.3145+7253G=
XR_926870.2:n.3145+7253G=
XR_926871.2:n.3013+7253G=
XR_926872.2:n.3145+7253G=
NM_138694.4:c.10500C= MANE Select NP_619639.3:p.Tyr3500=