Canonical Allele Identifier: CA1628469890

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627085C= , CM000668.2:g.51627085C=	GRCh38
NC_000006.11:g.51491883C= , CM000668.1:g.51491883C=	GRCh37
NC_000006.10:g.51599842C=	NCBI36
NG_008753.1:g.465541G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11697G= MANE Select	ENSP00000360158.3:p.Gln3899=
ENST00000371117.7:c.11697G=	ENSP00000360158.3:p.Gln3899=
NM_138694.3:c.11697G=	NP_619639.3:p.Gln3899=
XM_011514679.1:c.11697G=	XP_011512981.1:p.Gln3899=
XM_011514680.1:c.11697G=	XP_011512982.1:p.Gln3899=
XM_011514681.1:c.11568G=	XP_011512983.1:p.Gln3856=
XM_011514682.1:c.11559G=	XP_011512984.1:p.Gln3853=
XM_011514683.1:c.11055G=	XP_011512985.1:p.Gln3685=
XM_011514684.1:c.10986G=	XP_011512986.1:p.Gln3662=
XM_011514690.1:c.5772G=	XP_011512992.1:p.Gln1924=
XM_011514691.1:c.5772G=	XP_011512993.1:p.Gln1924=
XM_011514680.3:c.11697G=	XP_011512982.1:p.Gln3899=
XM_011514682.3:c.11559G=	XP_011512984.1:p.Gln3853=
XM_011514683.3:c.11055G=	XP_011512985.1:p.Gln3685=
XM_011514684.3:c.10986G=	XP_011512986.1:p.Gln3662=
XM_011514690.3:c.5772G=	XP_011512992.1:p.Gln1924=
XM_011514691.3:c.5772G=	XP_011512993.1:p.Gln1924=
XM_017010944.2:c.11697G=	XP_016866433.1:p.Gln3899=
XM_017010945.2:c.11622G=	XP_016866434.1:p.Gln3874=
XM_017010946.2:c.11502G=	XP_016866435.1:p.Gln3834=
XM_017010947.2:c.11433G=	XP_016866436.1:p.Gln3811=
XM_017010948.2:c.10986G=	XP_016866437.1:p.Gln3662=
XM_017010949.2:c.9837G=	XP_016866438.1:p.Gln3279=
NM_138694.4:c.11697G= MANE Select	NP_619639.3:p.Gln3899=