Canonical Allele Identifier: CA3850710
Gene: PKHD1 HGNC NCBI

Linked Data

dbSNP Id: rs748827743

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627020T>C , CM000668.2:g.51627020T>C GRCh38
NC_000006.11:g.51491818T>C , CM000668.1:g.51491818T>C GRCh37
NC_000006.10:g.51599777T>C NCBI36
NG_008753.1:g.465606A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11762A>G MANE Select ENSP00000360158.3:p.Lys3921Arg
ENST00000371117.7:c.11762A>G ENSP00000360158.3:p.Lys3921Arg
NM_138694.3:c.11762A>G NP_619639.3:p.Lys3921Arg
XM_011514679.1:c.11762A>G XP_011512981.1:p.Lys3921Arg
XM_011514680.1:c.11762A>G XP_011512982.1:p.Lys3921Arg
XM_011514681.1:c.11633A>G XP_011512983.1:p.Lys3878Arg
XM_011514682.1:c.11624A>G XP_011512984.1:p.Lys3875Arg
XM_011514683.1:c.11120A>G XP_011512985.1:p.Lys3707Arg
XM_011514684.1:c.11051A>G XP_011512986.1:p.Lys3684Arg
XM_011514690.1:c.5837A>G XP_011512992.1:p.Lys1946Arg
XM_011514691.1:c.5837A>G XP_011512993.1:p.Lys1946Arg
XM_011514680.3:c.11762A>G XP_011512982.1:p.Lys3921Arg
XM_011514682.3:c.11624A>G XP_011512984.1:p.Lys3875Arg
XM_011514683.3:c.11120A>G XP_011512985.1:p.Lys3707Arg
XM_011514684.3:c.11051A>G XP_011512986.1:p.Lys3684Arg
XM_011514690.3:c.5837A>G XP_011512992.1:p.Lys1946Arg
XM_011514691.3:c.5837A>G XP_011512993.1:p.Lys1946Arg
XM_017010944.2:c.11762A>G XP_016866433.1:p.Lys3921Arg
XM_017010945.2:c.11687A>G XP_016866434.1:p.Lys3896Arg
XM_017010946.2:c.11567A>G XP_016866435.1:p.Lys3856Arg
XM_017010947.2:c.11498A>G XP_016866436.1:p.Lys3833Arg
XM_017010948.2:c.11051A>G XP_016866437.1:p.Lys3684Arg
XM_017010949.2:c.9902A>G XP_016866438.1:p.Lys3301Arg
NM_138694.4:c.11762A>G MANE Select NP_619639.3:p.Lys3921Arg