Canonical Allele Identifier: CA1628439951
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659894A= , CM000668.2:g.51659894A= GRCh38
NC_000006.11:g.51524692A= , CM000668.1:g.51524692A= GRCh37
NC_000006.10:g.51632651A= NCBI36
NG_008753.1:g.432732T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.10232T= MANE Select ENSP00000360158.3:p.Val3411=
ENST00000371117.7:c.10232T= ENSP00000360158.3:p.Val3411=
NM_138694.3:c.10232T= NP_619639.3:p.Val3411=
XM_011514679.1:c.10232T= XP_011512981.1:p.Val3411=
XM_011514680.1:c.10232T= XP_011512982.1:p.Val3411=
XM_011514681.1:c.10103T= XP_011512983.1:p.Val3368=
XM_011514682.1:c.10094T= XP_011512984.1:p.Val3365=
XM_011514683.1:c.9590T= XP_011512985.1:p.Val3197=
XM_011514684.1:c.9521T= XP_011512986.1:p.Val3174=
XM_011514687.1:c.10157-10674T= XP_011512989.1:n.10157-10674T=
XM_011514690.1:c.4307T= XP_011512992.1:p.Val1436=
XM_011514691.1:c.4307T= XP_011512993.1:p.Val1436=
XR_926870.1:n.535+7521A=
XR_926871.1:n.403+7521A=
XR_926872.1:n.535+7521A=
XM_011514680.3:c.10232T= XP_011512982.1:p.Val3411=
XM_011514682.3:c.10094T= XP_011512984.1:p.Val3365=
XM_011514683.3:c.9590T= XP_011512985.1:p.Val3197=
XM_011514684.3:c.9521T= XP_011512986.1:p.Val3174=
XM_011514690.3:c.4307T= XP_011512992.1:p.Val1436=
XM_011514691.3:c.4307T= XP_011512993.1:p.Val1436=
XM_017010944.2:c.10232T= XP_016866433.1:p.Val3411=
XM_017010945.2:c.10157T= XP_016866434.1:p.Val3386=
XM_017010946.2:c.10037T= XP_016866435.1:p.Val3346=
XM_017010947.2:c.9968T= XP_016866436.1:p.Val3323=
XM_017010948.2:c.9521T= XP_016866437.1:p.Val3174=
XM_017010949.2:c.8372T= XP_016866438.1:p.Val2791=
XR_001743469.1:n.10508T=
XR_001744157.1:n.3145+7521A=
XR_926870.2:n.3145+7521A=
XR_926871.2:n.3013+7521A=
XR_926872.2:n.3145+7521A=
NM_138694.4:c.10232T= MANE Select NP_619639.3:p.Val3411=