Canonical Allele Identifier: CA275229
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51959901_51959902del , CM000668.2:g.51959901_51959902del GRCh38
NC_000006.11:g.51824699_51824700del , CM000668.1:g.51824699_51824700del GRCh37
NC_000006.10:g.51932658_51932659del NCBI36
NG_008753.1:g.132727_132728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.5879_5880del MANE Select ENSP00000360158.3:p.Thr1960LysfsTer9
ENST00000340994.4:c.5879_5880del ENSP00000341097.4:p.Thr1960LysfsTer9
ENST00000371117.7:c.5879_5880del ENSP00000360158.3:p.Thr1960LysfsTer9
NM_138694.3:c.5879_5880del NP_619639.3:p.Thr1960LysfsTer9
NM_170724.2:c.5879_5880del NP_733842.2:p.Thr1960LysfsTer9
XM_011514679.1:c.5879_5880del XP_011512981.1:p.Thr1960LysfsTer9
XM_011514680.1:c.5879_5880del XP_011512982.1:p.Thr1960LysfsTer9
XM_011514681.1:c.5879_5880del XP_011512983.1:p.Thr1960LysfsTer9
XM_011514682.1:c.5879_5880del XP_011512984.1:p.Thr1960LysfsTer9
XM_011514683.1:c.5237_5238del XP_011512985.1:p.Thr1746LysfsTer9
XM_011514684.1:c.5168_5169del XP_011512986.1:p.Thr1723LysfsTer9
XM_011514685.1:c.5879_5880del XP_011512987.1:p.Thr1960LysfsTer9
XM_011514686.1:c.5879_5880del XP_011512988.1:p.Thr1960LysfsTer9
XM_011514687.1:c.5879_5880del XP_011512989.1:p.Thr1960LysfsTer9
XM_011514688.1:c.5879_5880del XP_011512990.1:p.Thr1960LysfsTer9
XM_011514689.1:c.5879_5880del XP_011512991.1:p.Thr1960LysfsTer9
XM_011514690.1:c.-17-25577_-17-25576del XP_011512992.1:n.-17-25577_-17-25576del
XM_011514680.3:c.5879_5880del XP_011512982.1:p.Thr1960LysfsTer9
XM_011514682.3:c.5879_5880del XP_011512984.1:p.Thr1960LysfsTer9
XM_011514683.3:c.5237_5238del XP_011512985.1:p.Thr1746LysfsTer9
XM_011514684.3:c.5168_5169del XP_011512986.1:p.Thr1723LysfsTer9
XM_011514686.2:c.5879_5880del XP_011512988.1:p.Thr1960LysfsTer9
XM_011514688.2:c.5879_5880del XP_011512990.1:p.Thr1960LysfsTer9
XM_011514690.3:c.-17-25577_-17-25576del XP_011512992.1:n.-17-25577_-17-25576del
XM_017010944.2:c.5879_5880del XP_016866433.1:p.Thr1960LysfsTer9
XM_017010945.2:c.5804_5805del XP_016866434.1:p.Thr1935LysfsTer9
XM_017010946.2:c.5879_5880del XP_016866435.1:p.Thr1960LysfsTer9
XM_017010947.2:c.5615_5616del XP_016866436.1:p.Thr1872LysfsTer9
XM_017010948.2:c.5168_5169del XP_016866437.1:p.Thr1723LysfsTer9
XM_017010949.2:c.4019_4020del XP_016866438.1:p.Thr1340LysfsTer9
XM_017010950.1:c.5879_5880del XP_016866439.1:p.Thr1960LysfsTer9
XM_017010951.1:c.5879_5880del XP_016866440.1:p.Thr1960LysfsTer9
XM_017010952.1:c.5879_5880del XP_016866441.1:p.Thr1960LysfsTer9
XR_001743469.1:n.6155_6156del
NM_138694.4:c.5879_5880del MANE Select NP_619639.3:p.Thr1960LysfsTer9
NM_170724.3:c.5879_5880del NP_733842.2:p.Thr1960LysfsTer9