Canonical Allele Identifier: CA2679078633
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51748139_51748145del , CM000668.2:g.51748139_51748145del GRCh38
NC_000006.11:g.51612937_51612943del , CM000668.1:g.51612937_51612943del GRCh37
NC_000006.10:g.51720896_51720902del NCBI36
NG_008753.1:g.344486_344492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.9476_9482del MANE Select ENSP00000360158.3:p.Leu3159Ter
ENST00000340994.4:c.9476_9482del ENSP00000341097.4:p.Leu3159Ter
ENST00000371117.7:c.9476_9482del ENSP00000360158.3:p.Leu3159Ter
NM_138694.3:c.9476_9482del NP_619639.3:p.Leu3159Ter
NM_170724.2:c.9476_9482del NP_733842.2:p.Leu3159Ter
XM_011514679.1:c.9476_9482del XP_011512981.1:p.Leu3159Ter
XM_011514680.1:c.9476_9482del XP_011512982.1:p.Leu3159Ter
XM_011514681.1:c.9347_9353del XP_011512983.1:p.Leu3116Ter
XM_011514682.1:c.9338_9344del XP_011512984.1:p.Leu3113Ter
XM_011514683.1:c.8834_8840del XP_011512985.1:p.Leu2945Ter
XM_011514684.1:c.8765_8771del XP_011512986.1:p.Leu2922Ter
XM_011514685.1:c.9476_9482del XP_011512987.1:p.Leu3159Ter
XM_011514686.1:c.9476_9482del XP_011512988.1:p.Leu3159Ter
XM_011514687.1:c.9476_9482del XP_011512989.1:p.Leu3159Ter
XM_011514688.1:c.9476_9482del XP_011512990.1:p.Leu3159Ter
XM_011514690.1:c.3551_3557del XP_011512992.1:p.Leu1184Ter
XM_011514691.1:c.3551_3557del XP_011512993.1:p.Leu1184Ter
XM_011514680.3:c.9476_9482del XP_011512982.1:p.Leu3159Ter
XM_011514682.3:c.9338_9344del XP_011512984.1:p.Leu3113Ter
XM_011514683.3:c.8834_8840del XP_011512985.1:p.Leu2945Ter
XM_011514684.3:c.8765_8771del XP_011512986.1:p.Leu2922Ter
XM_011514686.2:c.9476_9482del XP_011512988.1:p.Leu3159Ter
XM_011514688.2:c.9476_9482del XP_011512990.1:p.Leu3159Ter
XM_011514690.3:c.3551_3557del XP_011512992.1:p.Leu1184Ter
XM_011514691.3:c.3551_3557del XP_011512993.1:p.Leu1184Ter
XM_017010944.2:c.9476_9482del XP_016866433.1:p.Leu3159Ter
XM_017010945.2:c.9401_9407del XP_016866434.1:p.Leu3134Ter
XM_017010946.2:c.9281_9287del XP_016866435.1:p.Leu3094Ter
XM_017010947.2:c.9212_9218del XP_016866436.1:p.Leu3071Ter
XM_017010948.2:c.8765_8771del XP_016866437.1:p.Leu2922Ter
XM_017010949.2:c.7616_7622del XP_016866438.1:p.Leu2539Ter
XM_017010950.1:c.9476_9482del XP_016866439.1:p.Leu3159Ter
XR_001743469.1:n.9752_9758del
NM_138694.4:c.9476_9482del MANE Select NP_619639.3:p.Leu3159Ter
NM_170724.3:c.9476_9482del NP_733842.2:p.Leu3159Ter