Canonical Allele Identifier: CA1628439366

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659606T= , CM000668.2:g.51659606T=	GRCh38
NC_000006.11:g.51524404T= , CM000668.1:g.51524404T=	GRCh37
NC_000006.10:g.51632363T=	NCBI36
NG_008753.1:g.433020A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10520A= MANE Select	ENSP00000360158.3:p.His3507=
ENST00000371117.7:c.10520A=	ENSP00000360158.3:p.His3507=
NM_138694.3:c.10520A=	NP_619639.3:p.His3507=
XM_011514679.1:c.10520A=	XP_011512981.1:p.His3507=
XM_011514680.1:c.10520A=	XP_011512982.1:p.His3507=
XM_011514681.1:c.10391A=	XP_011512983.1:p.His3464=
XM_011514682.1:c.10382A=	XP_011512984.1:p.His3461=
XM_011514683.1:c.9878A=	XP_011512985.1:p.His3293=
XM_011514684.1:c.9809A=	XP_011512986.1:p.His3270=
XM_011514687.1:c.10157-10386A=	XP_011512989.1:n.10157-10386A=
XM_011514690.1:c.4595A=	XP_011512992.1:p.His1532=
XM_011514691.1:c.4595A=	XP_011512993.1:p.His1532=
XR_926870.1:n.535+7233T=
XR_926871.1:n.403+7233T=
XR_926872.1:n.535+7233T=
XM_011514680.3:c.10520A=	XP_011512982.1:p.His3507=
XM_011514682.3:c.10382A=	XP_011512984.1:p.His3461=
XM_011514683.3:c.9878A=	XP_011512985.1:p.His3293=
XM_011514684.3:c.9809A=	XP_011512986.1:p.His3270=
XM_011514690.3:c.4595A=	XP_011512992.1:p.His1532=
XM_011514691.3:c.4595A=	XP_011512993.1:p.His1532=
XM_017010944.2:c.10520A=	XP_016866433.1:p.His3507=
XM_017010945.2:c.10445A=	XP_016866434.1:p.His3482=
XM_017010946.2:c.10325A=	XP_016866435.1:p.His3442=
XM_017010947.2:c.10256A=	XP_016866436.1:p.His3419=
XM_017010948.2:c.9809A=	XP_016866437.1:p.His3270=
XM_017010949.2:c.8660A=	XP_016866438.1:p.His2887=
XR_001743469.1:n.10796A=
XR_001744157.1:n.3145+7233T=
XR_926870.2:n.3145+7233T=
XR_926871.2:n.3013+7233T=
XR_926872.2:n.3145+7233T=
NM_138694.4:c.10520A= MANE Select	NP_619639.3:p.His3507=