Canonical Allele Identifier: CA1628440000

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659921C= , CM000668.2:g.51659921C=	GRCh38
NC_000006.11:g.51524719C= , CM000668.1:g.51524719C=	GRCh37
NC_000006.10:g.51632678C=	NCBI36
NG_008753.1:g.432705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10205G= MANE Select	ENSP00000360158.3:p.Gly3402=
ENST00000371117.7:c.10205G=	ENSP00000360158.3:p.Gly3402=
NM_138694.3:c.10205G=	NP_619639.3:p.Gly3402=
XM_011514679.1:c.10205G=	XP_011512981.1:p.Gly3402=
XM_011514680.1:c.10205G=	XP_011512982.1:p.Gly3402=
XM_011514681.1:c.10076G=	XP_011512983.1:p.Gly3359=
XM_011514682.1:c.10067G=	XP_011512984.1:p.Gly3356=
XM_011514683.1:c.9563G=	XP_011512985.1:p.Gly3188=
XM_011514684.1:c.9494G=	XP_011512986.1:p.Gly3165=
XM_011514687.1:c.10157-10701G=	XP_011512989.1:n.10157-10701G=
XM_011514690.1:c.4280G=	XP_011512992.1:p.Gly1427=
XM_011514691.1:c.4280G=	XP_011512993.1:p.Gly1427=
XR_926870.1:n.535+7548C=
XR_926871.1:n.403+7548C=
XR_926872.1:n.535+7548C=
XM_011514680.3:c.10205G=	XP_011512982.1:p.Gly3402=
XM_011514682.3:c.10067G=	XP_011512984.1:p.Gly3356=
XM_011514683.3:c.9563G=	XP_011512985.1:p.Gly3188=
XM_011514684.3:c.9494G=	XP_011512986.1:p.Gly3165=
XM_011514690.3:c.4280G=	XP_011512992.1:p.Gly1427=
XM_011514691.3:c.4280G=	XP_011512993.1:p.Gly1427=
XM_017010944.2:c.10205G=	XP_016866433.1:p.Gly3402=
XM_017010945.2:c.10130G=	XP_016866434.1:p.Gly3377=
XM_017010946.2:c.10010G=	XP_016866435.1:p.Gly3337=
XM_017010947.2:c.9941G=	XP_016866436.1:p.Gly3314=
XM_017010948.2:c.9494G=	XP_016866437.1:p.Gly3165=
XM_017010949.2:c.8345G=	XP_016866438.1:p.Gly2782=
XR_001743469.1:n.10481G=
XR_001744157.1:n.3145+7548C=
XR_926870.2:n.3145+7548C=
XR_926871.2:n.3013+7548C=
XR_926872.2:n.3145+7548C=
NM_138694.4:c.10205G= MANE Select	NP_619639.3:p.Gly3402=