Canonical Allele Identifier: CA1628439395
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659619G= , CM000668.2:g.51659619G= GRCh38
NC_000006.11:g.51524417G= , CM000668.1:g.51524417G= GRCh37
NC_000006.10:g.51632376G= NCBI36
NG_008753.1:g.433007C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.10507C= MANE Select ENSP00000360158.3:p.Leu3503=
ENST00000371117.7:c.10507C= ENSP00000360158.3:p.Leu3503=
NM_138694.3:c.10507C= NP_619639.3:p.Leu3503=
XM_011514679.1:c.10507C= XP_011512981.1:p.Leu3503=
XM_011514680.1:c.10507C= XP_011512982.1:p.Leu3503=
XM_011514681.1:c.10378C= XP_011512983.1:p.Leu3460=
XM_011514682.1:c.10369C= XP_011512984.1:p.Leu3457=
XM_011514683.1:c.9865C= XP_011512985.1:p.Leu3289=
XM_011514684.1:c.9796C= XP_011512986.1:p.Leu3266=
XM_011514687.1:c.10157-10399C= XP_011512989.1:n.10157-10399C=
XM_011514690.1:c.4582C= XP_011512992.1:p.Leu1528=
XM_011514691.1:c.4582C= XP_011512993.1:p.Leu1528=
XR_926870.1:n.535+7246G=
XR_926871.1:n.403+7246G=
XR_926872.1:n.535+7246G=
XM_011514680.3:c.10507C= XP_011512982.1:p.Leu3503=
XM_011514682.3:c.10369C= XP_011512984.1:p.Leu3457=
XM_011514683.3:c.9865C= XP_011512985.1:p.Leu3289=
XM_011514684.3:c.9796C= XP_011512986.1:p.Leu3266=
XM_011514690.3:c.4582C= XP_011512992.1:p.Leu1528=
XM_011514691.3:c.4582C= XP_011512993.1:p.Leu1528=
XM_017010944.2:c.10507C= XP_016866433.1:p.Leu3503=
XM_017010945.2:c.10432C= XP_016866434.1:p.Leu3478=
XM_017010946.2:c.10312C= XP_016866435.1:p.Leu3438=
XM_017010947.2:c.10243C= XP_016866436.1:p.Leu3415=
XM_017010948.2:c.9796C= XP_016866437.1:p.Leu3266=
XM_017010949.2:c.8647C= XP_016866438.1:p.Leu2883=
XR_001743469.1:n.10783C=
XR_001744157.1:n.3145+7246G=
XR_926870.2:n.3145+7246G=
XR_926871.2:n.3013+7246G=
XR_926872.2:n.3145+7246G=
NM_138694.4:c.10507C= MANE Select NP_619639.3:p.Leu3503=