Canonical Allele Identifier: CA1628438434
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659128A= , CM000668.2:g.51659128A= GRCh38
NC_000006.11:g.51523926A= , CM000668.1:g.51523926A= GRCh37
NC_000006.10:g.51631885A= NCBI36
NG_008753.1:g.433498T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.10998T= MANE Select ENSP00000360158.3:p.Ile3666=
ENST00000371117.7:c.10998T= ENSP00000360158.3:p.Ile3666=
NM_138694.3:c.10998T= NP_619639.3:p.Ile3666=
XM_011514679.1:c.10998T= XP_011512981.1:p.Ile3666=
XM_011514680.1:c.10998T= XP_011512982.1:p.Ile3666=
XM_011514681.1:c.10869T= XP_011512983.1:p.Ile3623=
XM_011514682.1:c.10860T= XP_011512984.1:p.Ile3620=
XM_011514683.1:c.10356T= XP_011512985.1:p.Ile3452=
XM_011514684.1:c.10287T= XP_011512986.1:p.Ile3429=
XM_011514687.1:c.10157-9908T= XP_011512989.1:n.10157-9908T=
XM_011514690.1:c.5073T= XP_011512992.1:p.Ile1691=
XM_011514691.1:c.5073T= XP_011512993.1:p.Ile1691=
XR_926870.1:n.535+6755A=
XR_926871.1:n.403+6755A=
XR_926872.1:n.535+6755A=
XM_011514680.3:c.10998T= XP_011512982.1:p.Ile3666=
XM_011514682.3:c.10860T= XP_011512984.1:p.Ile3620=
XM_011514683.3:c.10356T= XP_011512985.1:p.Ile3452=
XM_011514684.3:c.10287T= XP_011512986.1:p.Ile3429=
XM_011514690.3:c.5073T= XP_011512992.1:p.Ile1691=
XM_011514691.3:c.5073T= XP_011512993.1:p.Ile1691=
XM_017010944.2:c.10998T= XP_016866433.1:p.Ile3666=
XM_017010945.2:c.10923T= XP_016866434.1:p.Ile3641=
XM_017010946.2:c.10803T= XP_016866435.1:p.Ile3601=
XM_017010947.2:c.10734T= XP_016866436.1:p.Ile3578=
XM_017010948.2:c.10287T= XP_016866437.1:p.Ile3429=
XM_017010949.2:c.9138T= XP_016866438.1:p.Ile3046=
XR_001743469.1:n.11274T=
XR_001744157.1:n.3145+6755A=
XR_926870.2:n.3145+6755A=
XR_926871.2:n.3013+6755A=
XR_926872.2:n.3145+6755A=
NM_138694.4:c.10998T= MANE Select NP_619639.3:p.Ile3666=