Canonical Allele Identifier: CA364418572
Gene: PKHD1 HGNC NCBI

Linked Data

dbSNP Id: rs1767327118
gnomAD v4: 6-51627024-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627024T>C , CM000668.2:g.51627024T>C GRCh38
NC_000006.11:g.51491822T>C , CM000668.1:g.51491822T>C GRCh37
NC_000006.10:g.51599781T>C NCBI36
NG_008753.1:g.465602A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.11758A>G MANE Select ENSP00000360158.3:p.Lys3920Glu
ENST00000371117.7:c.11758A>G ENSP00000360158.3:p.Lys3920Glu
NM_138694.3:c.11758A>G NP_619639.3:p.Lys3920Glu
XM_011514679.1:c.11758A>G XP_011512981.1:p.Lys3920Glu
XM_011514680.1:c.11758A>G XP_011512982.1:p.Lys3920Glu
XM_011514681.1:c.11629A>G XP_011512983.1:p.Lys3877Glu
XM_011514682.1:c.11620A>G XP_011512984.1:p.Lys3874Glu
XM_011514683.1:c.11116A>G XP_011512985.1:p.Lys3706Glu
XM_011514684.1:c.11047A>G XP_011512986.1:p.Lys3683Glu
XM_011514690.1:c.5833A>G XP_011512992.1:p.Lys1945Glu
XM_011514691.1:c.5833A>G XP_011512993.1:p.Lys1945Glu
XM_011514680.3:c.11758A>G XP_011512982.1:p.Lys3920Glu
XM_011514682.3:c.11620A>G XP_011512984.1:p.Lys3874Glu
XM_011514683.3:c.11116A>G XP_011512985.1:p.Lys3706Glu
XM_011514684.3:c.11047A>G XP_011512986.1:p.Lys3683Glu
XM_011514690.3:c.5833A>G XP_011512992.1:p.Lys1945Glu
XM_011514691.3:c.5833A>G XP_011512993.1:p.Lys1945Glu
XM_017010944.2:c.11758A>G XP_016866433.1:p.Lys3920Glu
XM_017010945.2:c.11683A>G XP_016866434.1:p.Lys3895Glu
XM_017010946.2:c.11563A>G XP_016866435.1:p.Lys3855Glu
XM_017010947.2:c.11494A>G XP_016866436.1:p.Lys3832Glu
XM_017010948.2:c.11047A>G XP_016866437.1:p.Lys3683Glu
XM_017010949.2:c.9898A>G XP_016866438.1:p.Lys3300Glu
NM_138694.4:c.11758A>G MANE Select NP_619639.3:p.Lys3920Glu