Canonical Allele Identifier: CA1628438696

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659245G= , CM000668.2:g.51659245G=	GRCh38
NC_000006.11:g.51524043G= , CM000668.1:g.51524043G=	GRCh37
NC_000006.10:g.51632002G=	NCBI36
NG_008753.1:g.433381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10881C= MANE Select	ENSP00000360158.3:p.Cys3627=
ENST00000371117.7:c.10881C=	ENSP00000360158.3:p.Cys3627=
NM_138694.3:c.10881C=	NP_619639.3:p.Cys3627=
XM_011514679.1:c.10881C=	XP_011512981.1:p.Cys3627=
XM_011514680.1:c.10881C=	XP_011512982.1:p.Cys3627=
XM_011514681.1:c.10752C=	XP_011512983.1:p.Cys3584=
XM_011514682.1:c.10743C=	XP_011512984.1:p.Cys3581=
XM_011514683.1:c.10239C=	XP_011512985.1:p.Cys3413=
XM_011514684.1:c.10170C=	XP_011512986.1:p.Cys3390=
XM_011514687.1:c.10157-10025C=	XP_011512989.1:n.10157-10025C=
XM_011514690.1:c.4956C=	XP_011512992.1:p.Cys1652=
XM_011514691.1:c.4956C=	XP_011512993.1:p.Cys1652=
XR_926870.1:n.535+6872G=
XR_926871.1:n.403+6872G=
XR_926872.1:n.535+6872G=
XM_011514680.3:c.10881C=	XP_011512982.1:p.Cys3627=
XM_011514682.3:c.10743C=	XP_011512984.1:p.Cys3581=
XM_011514683.3:c.10239C=	XP_011512985.1:p.Cys3413=
XM_011514684.3:c.10170C=	XP_011512986.1:p.Cys3390=
XM_011514690.3:c.4956C=	XP_011512992.1:p.Cys1652=
XM_011514691.3:c.4956C=	XP_011512993.1:p.Cys1652=
XM_017010944.2:c.10881C=	XP_016866433.1:p.Cys3627=
XM_017010945.2:c.10806C=	XP_016866434.1:p.Cys3602=
XM_017010946.2:c.10686C=	XP_016866435.1:p.Cys3562=
XM_017010947.2:c.10617C=	XP_016866436.1:p.Cys3539=
XM_017010948.2:c.10170C=	XP_016866437.1:p.Cys3390=
XM_017010949.2:c.9021C=	XP_016866438.1:p.Cys3007=
XR_001743469.1:n.11157C=
XR_001744157.1:n.3145+6872G=
XR_926870.2:n.3145+6872G=
XR_926871.2:n.3013+6872G=
XR_926872.2:n.3145+6872G=
NM_138694.4:c.10881C= MANE Select	NP_619639.3:p.Cys3627=