Canonical Allele Identifier: CA1628647133

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52025076_52025077delinsAT , CM000668.2:g.52025076_52025077delinsAT	GRCh38
NC_000006.11:g.51889874_51889875delinsAT , CM000668.1:g.51889874_51889875delinsAT	GRCh37
NC_000006.10:g.51997833_51997834delinsAT	NCBI36
NG_008753.1:g.67549_67550delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.4733_4734delinsAT MANE Select	ENSP00000360158.3:p.Tyr1578=
ENST00000340994.4:c.4733_4734delinsAT	ENSP00000341097.4:p.Tyr1578=
ENST00000371117.7:c.4733_4734delinsAT	ENSP00000360158.3:p.Tyr1578=
NM_138694.3:c.4733_4734delinsAT	NP_619639.3:p.Tyr1578=
NM_170724.2:c.4733_4734delinsAT	NP_733842.2:p.Tyr1578=
XM_011514679.1:c.4733_4734delinsAT	XP_011512981.1:p.Tyr1578=
XM_011514680.1:c.4733_4734delinsAT	XP_011512982.1:p.Tyr1578=
XM_011514681.1:c.4733_4734delinsAT	XP_011512983.1:p.Tyr1578=
XM_011514682.1:c.4733_4734delinsAT	XP_011512984.1:p.Tyr1578=
XM_011514683.1:c.4102-11_4102-10delinsAT	XP_011512985.1:n.4102-11_4102-10delinsAT
XM_011514684.1:c.4022_4023delinsAT	XP_011512986.1:p.Tyr1341=
XM_011514685.1:c.4733_4734delinsAT	XP_011512987.1:p.Tyr1578=
XM_011514686.1:c.4733_4734delinsAT	XP_011512988.1:p.Tyr1578=
XM_011514687.1:c.4733_4734delinsAT	XP_011512989.1:p.Tyr1578=
XM_011514688.1:c.4733_4734delinsAT	XP_011512990.1:p.Tyr1578=
XM_011514689.1:c.4733_4734delinsAT	XP_011512991.1:p.Tyr1578=
XM_011514680.3:c.4733_4734delinsAT	XP_011512982.1:p.Tyr1578=
XM_011514682.3:c.4733_4734delinsAT	XP_011512984.1:p.Tyr1578=
XM_011514683.3:c.4102-11_4102-10delinsAT	XP_011512985.1:n.4102-11_4102-10delinsAT
XM_011514684.3:c.4022_4023delinsAT	XP_011512986.1:p.Tyr1341=
XM_011514686.2:c.4733_4734delinsAT	XP_011512988.1:p.Tyr1578=
XM_011514688.2:c.4733_4734delinsAT	XP_011512990.1:p.Tyr1578=
XM_017010944.2:c.4733_4734delinsAT	XP_016866433.1:p.Tyr1578=
XM_017010945.2:c.4658_4659delinsAT	XP_016866434.1:p.Tyr1553=
XM_017010946.2:c.4733_4734delinsAT	XP_016866435.1:p.Tyr1578=
XM_017010947.2:c.4469_4470delinsAT	XP_016866436.1:p.Tyr1490=
XM_017010948.2:c.4022_4023delinsAT	XP_016866437.1:p.Tyr1341=
XM_017010949.2:c.2873_2874delinsAT	XP_016866438.1:p.Tyr958=
XM_017010950.1:c.4733_4734delinsAT	XP_016866439.1:p.Tyr1578=
XM_017010951.1:c.4733_4734delinsAT	XP_016866440.1:p.Tyr1578=
XM_017010952.1:c.4733_4734delinsAT	XP_016866441.1:p.Tyr1578=
XR_001743469.1:n.5009_5010delinsAT
NM_138694.4:c.4733_4734delinsAT MANE Select	NP_619639.3:p.Tyr1578=
NM_170724.3:c.4733_4734delinsAT	NP_733842.2:p.Tyr1578=