Canonical Allele Identifier: CA1628438339
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659059C= , CM000668.2:g.51659059C= GRCh38
NC_000006.11:g.51523857C= , CM000668.1:g.51523857C= GRCh37
NC_000006.10:g.51631816C= NCBI36
NG_008753.1:g.433567G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.11067G= MANE Select ENSP00000360158.3:p.Leu3689=
ENST00000371117.7:c.11067G= ENSP00000360158.3:p.Leu3689=
NM_138694.3:c.11067G= NP_619639.3:p.Leu3689=
XM_011514679.1:c.11067G= XP_011512981.1:p.Leu3689=
XM_011514680.1:c.11067G= XP_011512982.1:p.Leu3689=
XM_011514681.1:c.10938G= XP_011512983.1:p.Leu3646=
XM_011514682.1:c.10929G= XP_011512984.1:p.Leu3643=
XM_011514683.1:c.10425G= XP_011512985.1:p.Leu3475=
XM_011514684.1:c.10356G= XP_011512986.1:p.Leu3452=
XM_011514687.1:c.10157-9839G= XP_011512989.1:n.10157-9839G=
XM_011514690.1:c.5142G= XP_011512992.1:p.Leu1714=
XM_011514691.1:c.5142G= XP_011512993.1:p.Leu1714=
XR_926870.1:n.535+6686C=
XR_926871.1:n.403+6686C=
XR_926872.1:n.535+6686C=
XM_011514680.3:c.11067G= XP_011512982.1:p.Leu3689=
XM_011514682.3:c.10929G= XP_011512984.1:p.Leu3643=
XM_011514683.3:c.10425G= XP_011512985.1:p.Leu3475=
XM_011514684.3:c.10356G= XP_011512986.1:p.Leu3452=
XM_011514690.3:c.5142G= XP_011512992.1:p.Leu1714=
XM_011514691.3:c.5142G= XP_011512993.1:p.Leu1714=
XM_017010944.2:c.11067G= XP_016866433.1:p.Leu3689=
XM_017010945.2:c.10992G= XP_016866434.1:p.Leu3664=
XM_017010946.2:c.10872G= XP_016866435.1:p.Leu3624=
XM_017010947.2:c.10803G= XP_016866436.1:p.Leu3601=
XM_017010948.2:c.10356G= XP_016866437.1:p.Leu3452=
XM_017010949.2:c.9207G= XP_016866438.1:p.Leu3069=
XR_001743469.1:n.11343G=
XR_001744157.1:n.3145+6686C=
XR_926870.2:n.3145+6686C=
XR_926871.2:n.3013+6686C=
XR_926872.2:n.3145+6686C=
NM_138694.4:c.11067G= MANE Select NP_619639.3:p.Leu3689=