Canonical Allele Identifier: CA2679084934
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52024947del , CM000668.2:g.52024947del GRCh38
NC_000006.11:g.51889745del , CM000668.1:g.51889745del GRCh37
NC_000006.10:g.51997704del NCBI36
NG_008753.1:g.67679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.4863del MANE Select ENSP00000360158.3:p.Glu1621AspfsTer18
ENST00000340994.4:c.4863del ENSP00000341097.4:p.Glu1621AspfsTer18
ENST00000371117.7:c.4863del ENSP00000360158.3:p.Glu1621AspfsTer18
NM_138694.3:c.4863del NP_619639.3:p.Glu1621AspfsTer18
NM_170724.2:c.4863del NP_733842.2:p.Glu1621AspfsTer18
XM_011514679.1:c.4863del XP_011512981.1:p.Glu1621AspfsTer18
XM_011514680.1:c.4863del XP_011512982.1:p.Glu1621AspfsTer18
XM_011514681.1:c.4863del XP_011512983.1:p.Glu1621AspfsTer18
XM_011514682.1:c.4863del XP_011512984.1:p.Glu1621AspfsTer18
XM_011514683.1:c.4221del XP_011512985.1:p.Glu1407AspfsTer18
XM_011514684.1:c.4152del XP_011512986.1:p.Glu1384AspfsTer18
XM_011514685.1:c.4863del XP_011512987.1:p.Glu1621AspfsTer18
XM_011514686.1:c.4863del XP_011512988.1:p.Glu1621AspfsTer18
XM_011514687.1:c.4863del XP_011512989.1:p.Glu1621AspfsTer18
XM_011514688.1:c.4863del XP_011512990.1:p.Glu1621AspfsTer18
XM_011514689.1:c.4863del XP_011512991.1:p.Glu1621AspfsTer18
XM_011514680.3:c.4863del XP_011512982.1:p.Glu1621AspfsTer18
XM_011514682.3:c.4863del XP_011512984.1:p.Glu1621AspfsTer18
XM_011514683.3:c.4221del XP_011512985.1:p.Glu1407AspfsTer18
XM_011514684.3:c.4152del XP_011512986.1:p.Glu1384AspfsTer18
XM_011514686.2:c.4863del XP_011512988.1:p.Glu1621AspfsTer18
XM_011514688.2:c.4863del XP_011512990.1:p.Glu1621AspfsTer18
XM_017010944.2:c.4863del XP_016866433.1:p.Glu1621AspfsTer18
XM_017010945.2:c.4788del XP_016866434.1:p.Glu1596AspfsTer18
XM_017010946.2:c.4863del XP_016866435.1:p.Glu1621AspfsTer18
XM_017010947.2:c.4599del XP_016866436.1:p.Glu1533AspfsTer18
XM_017010948.2:c.4152del XP_016866437.1:p.Glu1384AspfsTer18
XM_017010949.2:c.3003del XP_016866438.1:p.Glu1001AspfsTer18
XM_017010950.1:c.4863del XP_016866439.1:p.Glu1621AspfsTer18
XM_017010951.1:c.4863del XP_016866440.1:p.Glu1621AspfsTer18
XM_017010952.1:c.4863del XP_016866441.1:p.Glu1621AspfsTer18
XR_001743469.1:n.5139del
NM_138694.4:c.4863del MANE Select NP_619639.3:p.Glu1621AspfsTer18
NM_170724.3:c.4863del NP_733842.2:p.Glu1621AspfsTer18