Canonical Allele Identifier: CA1628439593
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659702T= , CM000668.2:g.51659702T= GRCh38
NC_000006.11:g.51524500T= , CM000668.1:g.51524500T= GRCh37
NC_000006.10:g.51632459T= NCBI36
NG_008753.1:g.432924A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.10424A= MANE Select ENSP00000360158.3:p.Asp3475=
ENST00000371117.7:c.10424A= ENSP00000360158.3:p.Asp3475=
NM_138694.3:c.10424A= NP_619639.3:p.Asp3475=
XM_011514679.1:c.10424A= XP_011512981.1:p.Asp3475=
XM_011514680.1:c.10424A= XP_011512982.1:p.Asp3475=
XM_011514681.1:c.10295A= XP_011512983.1:p.Asp3432=
XM_011514682.1:c.10286A= XP_011512984.1:p.Asp3429=
XM_011514683.1:c.9782A= XP_011512985.1:p.Asp3261=
XM_011514684.1:c.9713A= XP_011512986.1:p.Asp3238=
XM_011514687.1:c.10157-10482A= XP_011512989.1:n.10157-10482A=
XM_011514690.1:c.4499A= XP_011512992.1:p.Asp1500=
XM_011514691.1:c.4499A= XP_011512993.1:p.Asp1500=
XR_926870.1:n.535+7329T=
XR_926871.1:n.403+7329T=
XR_926872.1:n.535+7329T=
XM_011514680.3:c.10424A= XP_011512982.1:p.Asp3475=
XM_011514682.3:c.10286A= XP_011512984.1:p.Asp3429=
XM_011514683.3:c.9782A= XP_011512985.1:p.Asp3261=
XM_011514684.3:c.9713A= XP_011512986.1:p.Asp3238=
XM_011514690.3:c.4499A= XP_011512992.1:p.Asp1500=
XM_011514691.3:c.4499A= XP_011512993.1:p.Asp1500=
XM_017010944.2:c.10424A= XP_016866433.1:p.Asp3475=
XM_017010945.2:c.10349A= XP_016866434.1:p.Asp3450=
XM_017010946.2:c.10229A= XP_016866435.1:p.Asp3410=
XM_017010947.2:c.10160A= XP_016866436.1:p.Asp3387=
XM_017010948.2:c.9713A= XP_016866437.1:p.Asp3238=
XM_017010949.2:c.8564A= XP_016866438.1:p.Asp2855=
XR_001743469.1:n.10700A=
XR_001744157.1:n.3145+7329T=
XR_926870.2:n.3145+7329T=
XR_926871.2:n.3013+7329T=
XR_926872.2:n.3145+7329T=
NM_138694.4:c.10424A= MANE Select NP_619639.3:p.Asp3475=