Canonical Allele Identifier: CA1628439306

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659586A= , CM000668.2:g.51659586A=	GRCh38
NC_000006.11:g.51524384A= , CM000668.1:g.51524384A=	GRCh37
NC_000006.10:g.51632343A=	NCBI36
NG_008753.1:g.433040T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10540T= MANE Select	ENSP00000360158.3:p.Phe3514=
ENST00000371117.7:c.10540T=	ENSP00000360158.3:p.Phe3514=
NM_138694.3:c.10540T=	NP_619639.3:p.Phe3514=
XM_011514679.1:c.10540T=	XP_011512981.1:p.Phe3514=
XM_011514680.1:c.10540T=	XP_011512982.1:p.Phe3514=
XM_011514681.1:c.10411T=	XP_011512983.1:p.Phe3471=
XM_011514682.1:c.10402T=	XP_011512984.1:p.Phe3468=
XM_011514683.1:c.9898T=	XP_011512985.1:p.Phe3300=
XM_011514684.1:c.9829T=	XP_011512986.1:p.Phe3277=
XM_011514687.1:c.10157-10366T=	XP_011512989.1:n.10157-10366T=
XM_011514690.1:c.4615T=	XP_011512992.1:p.Phe1539=
XM_011514691.1:c.4615T=	XP_011512993.1:p.Phe1539=
XR_926870.1:n.535+7213A=
XR_926871.1:n.403+7213A=
XR_926872.1:n.535+7213A=
XM_011514680.3:c.10540T=	XP_011512982.1:p.Phe3514=
XM_011514682.3:c.10402T=	XP_011512984.1:p.Phe3468=
XM_011514683.3:c.9898T=	XP_011512985.1:p.Phe3300=
XM_011514684.3:c.9829T=	XP_011512986.1:p.Phe3277=
XM_011514690.3:c.4615T=	XP_011512992.1:p.Phe1539=
XM_011514691.3:c.4615T=	XP_011512993.1:p.Phe1539=
XM_017010944.2:c.10540T=	XP_016866433.1:p.Phe3514=
XM_017010945.2:c.10465T=	XP_016866434.1:p.Phe3489=
XM_017010946.2:c.10345T=	XP_016866435.1:p.Phe3449=
XM_017010947.2:c.10276T=	XP_016866436.1:p.Phe3426=
XM_017010948.2:c.9829T=	XP_016866437.1:p.Phe3277=
XM_017010949.2:c.8680T=	XP_016866438.1:p.Phe2894=
XR_001743469.1:n.10816T=
XR_001744157.1:n.3145+7213A=
XR_926870.2:n.3145+7213A=
XR_926871.2:n.3013+7213A=
XR_926872.2:n.3145+7213A=
NM_138694.4:c.10540T= MANE Select	NP_619639.3:p.Phe3514=