Canonical Allele Identifier: CA1628438679

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659234T= , CM000668.2:g.51659234T=	GRCh38
NC_000006.11:g.51524032T= , CM000668.1:g.51524032T=	GRCh37
NC_000006.10:g.51631991T=	NCBI36
NG_008753.1:g.433392A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10892A= MANE Select	ENSP00000360158.3:p.Tyr3631=
ENST00000371117.7:c.10892A=	ENSP00000360158.3:p.Tyr3631=
NM_138694.3:c.10892A=	NP_619639.3:p.Tyr3631=
XM_011514679.1:c.10892A=	XP_011512981.1:p.Tyr3631=
XM_011514680.1:c.10892A=	XP_011512982.1:p.Tyr3631=
XM_011514681.1:c.10763A=	XP_011512983.1:p.Tyr3588=
XM_011514682.1:c.10754A=	XP_011512984.1:p.Tyr3585=
XM_011514683.1:c.10250A=	XP_011512985.1:p.Tyr3417=
XM_011514684.1:c.10181A=	XP_011512986.1:p.Tyr3394=
XM_011514687.1:c.10157-10014A=	XP_011512989.1:n.10157-10014A=
XM_011514690.1:c.4967A=	XP_011512992.1:p.Tyr1656=
XM_011514691.1:c.4967A=	XP_011512993.1:p.Tyr1656=
XR_926870.1:n.535+6861T=
XR_926871.1:n.403+6861T=
XR_926872.1:n.535+6861T=
XM_011514680.3:c.10892A=	XP_011512982.1:p.Tyr3631=
XM_011514682.3:c.10754A=	XP_011512984.1:p.Tyr3585=
XM_011514683.3:c.10250A=	XP_011512985.1:p.Tyr3417=
XM_011514684.3:c.10181A=	XP_011512986.1:p.Tyr3394=
XM_011514690.3:c.4967A=	XP_011512992.1:p.Tyr1656=
XM_011514691.3:c.4967A=	XP_011512993.1:p.Tyr1656=
XM_017010944.2:c.10892A=	XP_016866433.1:p.Tyr3631=
XM_017010945.2:c.10817A=	XP_016866434.1:p.Tyr3606=
XM_017010946.2:c.10697A=	XP_016866435.1:p.Tyr3566=
XM_017010947.2:c.10628A=	XP_016866436.1:p.Tyr3543=
XM_017010948.2:c.10181A=	XP_016866437.1:p.Tyr3394=
XM_017010949.2:c.9032A=	XP_016866438.1:p.Tyr3011=
XR_001743469.1:n.11168A=
XR_001744157.1:n.3145+6861T=
XR_926870.2:n.3145+6861T=
XR_926871.2:n.3013+6861T=
XR_926872.2:n.3145+6861T=
NM_138694.4:c.10892A= MANE Select	NP_619639.3:p.Tyr3631=