Canonical Allele Identifier: CA1628469936

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627099T= , CM000668.2:g.51627099T=	GRCh38
NC_000006.11:g.51491897T= , CM000668.1:g.51491897T=	GRCh37
NC_000006.10:g.51599856T=	NCBI36
NG_008753.1:g.465527A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11683A= MANE Select	ENSP00000360158.3:p.Ile3895=
ENST00000371117.7:c.11683A=	ENSP00000360158.3:p.Ile3895=
NM_138694.3:c.11683A=	NP_619639.3:p.Ile3895=
XM_011514679.1:c.11683A=	XP_011512981.1:p.Ile3895=
XM_011514680.1:c.11683A=	XP_011512982.1:p.Ile3895=
XM_011514681.1:c.11554A=	XP_011512983.1:p.Ile3852=
XM_011514682.1:c.11545A=	XP_011512984.1:p.Ile3849=
XM_011514683.1:c.11041A=	XP_011512985.1:p.Ile3681=
XM_011514684.1:c.10972A=	XP_011512986.1:p.Ile3658=
XM_011514690.1:c.5758A=	XP_011512992.1:p.Ile1920=
XM_011514691.1:c.5758A=	XP_011512993.1:p.Ile1920=
XM_011514680.3:c.11683A=	XP_011512982.1:p.Ile3895=
XM_011514682.3:c.11545A=	XP_011512984.1:p.Ile3849=
XM_011514683.3:c.11041A=	XP_011512985.1:p.Ile3681=
XM_011514684.3:c.10972A=	XP_011512986.1:p.Ile3658=
XM_011514690.3:c.5758A=	XP_011512992.1:p.Ile1920=
XM_011514691.3:c.5758A=	XP_011512993.1:p.Ile1920=
XM_017010944.2:c.11683A=	XP_016866433.1:p.Ile3895=
XM_017010945.2:c.11608A=	XP_016866434.1:p.Ile3870=
XM_017010946.2:c.11488A=	XP_016866435.1:p.Ile3830=
XM_017010947.2:c.11419A=	XP_016866436.1:p.Ile3807=
XM_017010948.2:c.10972A=	XP_016866437.1:p.Ile3658=
XM_017010949.2:c.9823A=	XP_016866438.1:p.Ile3275=
NM_138694.4:c.11683A= MANE Select	NP_619639.3:p.Ile3895=