Canonical Allele Identifier: CA1628438717

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659254A= , CM000668.2:g.51659254A=	GRCh38
NC_000006.11:g.51524052A= , CM000668.1:g.51524052A=	GRCh37
NC_000006.10:g.51632011A=	NCBI36
NG_008753.1:g.433372T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10872T= MANE Select	ENSP00000360158.3:p.Thr3624=
ENST00000371117.7:c.10872T=	ENSP00000360158.3:p.Thr3624=
NM_138694.3:c.10872T=	NP_619639.3:p.Thr3624=
XM_011514679.1:c.10872T=	XP_011512981.1:p.Thr3624=
XM_011514680.1:c.10872T=	XP_011512982.1:p.Thr3624=
XM_011514681.1:c.10743T=	XP_011512983.1:p.Thr3581=
XM_011514682.1:c.10734T=	XP_011512984.1:p.Thr3578=
XM_011514683.1:c.10230T=	XP_011512985.1:p.Thr3410=
XM_011514684.1:c.10161T=	XP_011512986.1:p.Thr3387=
XM_011514687.1:c.10157-10034T=	XP_011512989.1:n.10157-10034T=
XM_011514690.1:c.4947T=	XP_011512992.1:p.Thr1649=
XM_011514691.1:c.4947T=	XP_011512993.1:p.Thr1649=
XR_926870.1:n.535+6881A=
XR_926871.1:n.403+6881A=
XR_926872.1:n.535+6881A=
XM_011514680.3:c.10872T=	XP_011512982.1:p.Thr3624=
XM_011514682.3:c.10734T=	XP_011512984.1:p.Thr3578=
XM_011514683.3:c.10230T=	XP_011512985.1:p.Thr3410=
XM_011514684.3:c.10161T=	XP_011512986.1:p.Thr3387=
XM_011514690.3:c.4947T=	XP_011512992.1:p.Thr1649=
XM_011514691.3:c.4947T=	XP_011512993.1:p.Thr1649=
XM_017010944.2:c.10872T=	XP_016866433.1:p.Thr3624=
XM_017010945.2:c.10797T=	XP_016866434.1:p.Thr3599=
XM_017010946.2:c.10677T=	XP_016866435.1:p.Thr3559=
XM_017010947.2:c.10608T=	XP_016866436.1:p.Thr3536=
XM_017010948.2:c.10161T=	XP_016866437.1:p.Thr3387=
XM_017010949.2:c.9012T=	XP_016866438.1:p.Thr3004=
XR_001743469.1:n.11148T=
XR_001744157.1:n.3145+6881A=
XR_926870.2:n.3145+6881A=
XR_926871.2:n.3013+6881A=
XR_926872.2:n.3145+6881A=
NM_138694.4:c.10872T= MANE Select	NP_619639.3:p.Thr3624=