Canonical Allele Identifier: CA1088988662

Gene: PKHD1

Linked Data

• gnomAD v3: 6-52043503-T-TG
• gnomAD v4: 6-52043503-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52043503_52043504insG , CM000668.2:g.52043503_52043504insG	GRCh38
NC_000006.11:g.51908301_51908302insG , CM000668.1:g.51908301_51908302insG	GRCh37
NC_000006.10:g.52016260_52016261insG	NCBI36
NG_008753.1:g.49122_49123insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.2821+121_2821+122insC MANE Select	ENSP00000360158.3:n.2821+121_2821+122insC
ENST00000340994.4:c.2821+121_2821+122insC	ENSP00000341097.4:n.2821+121_2821+122insC
ENST00000371117.7:c.2821+121_2821+122insC	ENSP00000360158.3:n.2821+121_2821+122insC
NM_138694.3:c.2821+121_2821+122insC	NP_619639.3:n.2821+121_2821+122insC
NM_170724.2:c.2821+121_2821+122insC	NP_733842.2:n.2821+121_2821+122insC
XM_011514679.1:c.2821+121_2821+122insC	XP_011512981.1:n.2821+121_2821+122insC
XM_011514680.1:c.2821+121_2821+122insC	XP_011512982.1:n.2821+121_2821+122insC
XM_011514681.1:c.2821+121_2821+122insC	XP_011512983.1:n.2821+121_2821+122insC
XM_011514682.1:c.2821+121_2821+122insC	XP_011512984.1:n.2821+121_2821+122insC
XM_011514683.1:c.2821+121_2821+122insC	XP_011512985.1:n.2821+121_2821+122insC
XM_011514684.1:c.2110+121_2110+122insC	XP_011512986.1:n.2110+121_2110+122insC
XM_011514685.1:c.2821+121_2821+122insC	XP_011512987.1:n.2821+121_2821+122insC
XM_011514686.1:c.2821+121_2821+122insC	XP_011512988.1:n.2821+121_2821+122insC
XM_011514687.1:c.2821+121_2821+122insC	XP_011512989.1:n.2821+121_2821+122insC
XM_011514688.1:c.2821+121_2821+122insC	XP_011512990.1:n.2821+121_2821+122insC
XM_011514689.1:c.2821+121_2821+122insC	XP_011512991.1:n.2821+121_2821+122insC
XM_011514680.3:c.2821+121_2821+122insC	XP_011512982.1:n.2821+121_2821+122insC
XM_011514682.3:c.2821+121_2821+122insC	XP_011512984.1:n.2821+121_2821+122insC
XM_011514683.3:c.2821+121_2821+122insC	XP_011512985.1:n.2821+121_2821+122insC
XM_011514684.3:c.2110+121_2110+122insC	XP_011512986.1:n.2110+121_2110+122insC
XM_011514686.2:c.2821+121_2821+122insC	XP_011512988.1:n.2821+121_2821+122insC
XM_011514688.2:c.2821+121_2821+122insC	XP_011512990.1:n.2821+121_2821+122insC
XM_017010944.2:c.2821+121_2821+122insC	XP_016866433.1:n.2821+121_2821+122insC
XM_017010945.2:c.2746+121_2746+122insC	XP_016866434.1:n.2746+121_2746+122insC
XM_017010946.2:c.2821+121_2821+122insC	XP_016866435.1:n.2821+121_2821+122insC
XM_017010947.2:c.2821+121_2821+122insC	XP_016866436.1:n.2821+121_2821+122insC
XM_017010948.2:c.2110+121_2110+122insC	XP_016866437.1:n.2110+121_2110+122insC
XM_017010949.2:c.961+121_961+122insC	XP_016866438.1:n.961+121_961+122insC
XM_017010950.1:c.2821+121_2821+122insC	XP_016866439.1:n.2821+121_2821+122insC
XM_017010951.1:c.2821+121_2821+122insC	XP_016866440.1:n.2821+121_2821+122insC
XM_017010952.1:c.2821+121_2821+122insC	XP_016866441.1:n.2821+121_2821+122insC
XR_001743469.1:n.3097+121_3097+122insC
NM_138694.4:c.2821+121_2821+122insC MANE Select	NP_619639.3:n.2821+121_2821+122insC
NM_170724.3:c.2821+121_2821+122insC	NP_733842.2:n.2821+121_2821+122insC