Canonical Allele Identifier: CA2695206434
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51748566_51748568del , CM000668.2:g.51748566_51748568del GRCh38
NC_000006.11:g.51613364_51613366del , CM000668.1:g.51613364_51613366del GRCh37
NC_000006.10:g.51721323_51721325del NCBI36
NG_008753.1:g.344061_344063del

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.9051_9053del MANE Select ENSP00000360158.3:p.Ser3018del
ENST00000340994.4:c.9051_9053del ENSP00000341097.4:p.Ser3018del
ENST00000371117.7:c.9051_9053del ENSP00000360158.3:p.Ser3018del
NM_138694.3:c.9051_9053del NP_619639.3:p.Ser3018del
NM_170724.2:c.9051_9053del NP_733842.2:p.Ser3018del
XM_011514679.1:c.9051_9053del XP_011512981.1:p.Ser3018del
XM_011514680.1:c.9051_9053del XP_011512982.1:p.Ser3018del
XM_011514681.1:c.8922_8924del XP_011512983.1:p.Ser2975del
XM_011514682.1:c.8913_8915del XP_011512984.1:p.Ser2972del
XM_011514683.1:c.8409_8411del XP_011512985.1:p.Ser2804del
XM_011514684.1:c.8340_8342del XP_011512986.1:p.Ser2781del
XM_011514685.1:c.9051_9053del XP_011512987.1:p.Ser3018del
XM_011514686.1:c.9051_9053del XP_011512988.1:p.Ser3018del
XM_011514687.1:c.9051_9053del XP_011512989.1:p.Ser3018del
XM_011514688.1:c.9051_9053del XP_011512990.1:p.Ser3018del
XM_011514690.1:c.3126_3128del XP_011512992.1:p.Ser1043del
XM_011514691.1:c.3126_3128del XP_011512993.1:p.Ser1043del
XM_011514680.3:c.9051_9053del XP_011512982.1:p.Ser3018del
XM_011514682.3:c.8913_8915del XP_011512984.1:p.Ser2972del
XM_011514683.3:c.8409_8411del XP_011512985.1:p.Ser2804del
XM_011514684.3:c.8340_8342del XP_011512986.1:p.Ser2781del
XM_011514686.2:c.9051_9053del XP_011512988.1:p.Ser3018del
XM_011514688.2:c.9051_9053del XP_011512990.1:p.Ser3018del
XM_011514690.3:c.3126_3128del XP_011512992.1:p.Ser1043del
XM_011514691.3:c.3126_3128del XP_011512993.1:p.Ser1043del
XM_017010944.2:c.9051_9053del XP_016866433.1:p.Ser3018del
XM_017010945.2:c.8976_8978del XP_016866434.1:p.Ser2993del
XM_017010946.2:c.8856_8858del XP_016866435.1:p.Ser2953del
XM_017010947.2:c.8787_8789del XP_016866436.1:p.Ser2930del
XM_017010948.2:c.8340_8342del XP_016866437.1:p.Ser2781del
XM_017010949.2:c.7191_7193del XP_016866438.1:p.Ser2398del
XM_017010950.1:c.9051_9053del XP_016866439.1:p.Ser3018del
XR_001743469.1:n.9327_9329del
NM_138694.4:c.9051_9053del MANE Select NP_619639.3:p.Ser3018del
NM_170724.3:c.9051_9053del NP_733842.2:p.Ser3018del