Canonical Allele Identifier: CA450613185

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524538G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659740G>T , CM000668.2:g.51659740G>T	GRCh38
NC_000006.11:g.51524538G>T , CM000668.1:g.51524538G>T	GRCh37
NC_000006.10:g.51632497G>T	NCBI36
NG_008753.1:g.432886C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10386C>A MANE Select	ENSP00000360158.3:p.Ile3462=
ENST00000371117.7:c.10386C>A	ENSP00000360158.3:p.Ile3462=
NM_138694.3:c.10386C>A	NP_619639.3:p.Ile3462=
XM_011514679.1:c.10386C>A	XP_011512981.1:p.Ile3462=
XM_011514680.1:c.10386C>A	XP_011512982.1:p.Ile3462=
XM_011514681.1:c.10257C>A	XP_011512983.1:p.Ile3419=
XM_011514682.1:c.10248C>A	XP_011512984.1:p.Ile3416=
XM_011514683.1:c.9744C>A	XP_011512985.1:p.Ile3248=
XM_011514684.1:c.9675C>A	XP_011512986.1:p.Ile3225=
XM_011514687.1:c.10157-10520C>A	XP_011512989.1:n.10157-10520C>A
XM_011514690.1:c.4461C>A	XP_011512992.1:p.Ile1487=
XM_011514691.1:c.4461C>A	XP_011512993.1:p.Ile1487=
XR_926870.1:n.535+7367G>T
XR_926871.1:n.403+7367G>T
XR_926872.1:n.535+7367G>T
XM_011514680.3:c.10386C>A	XP_011512982.1:p.Ile3462=
XM_011514682.3:c.10248C>A	XP_011512984.1:p.Ile3416=
XM_011514683.3:c.9744C>A	XP_011512985.1:p.Ile3248=
XM_011514684.3:c.9675C>A	XP_011512986.1:p.Ile3225=
XM_011514690.3:c.4461C>A	XP_011512992.1:p.Ile1487=
XM_011514691.3:c.4461C>A	XP_011512993.1:p.Ile1487=
XM_017010944.2:c.10386C>A	XP_016866433.1:p.Ile3462=
XM_017010945.2:c.10311C>A	XP_016866434.1:p.Ile3437=
XM_017010946.2:c.10191C>A	XP_016866435.1:p.Ile3397=
XM_017010947.2:c.10122C>A	XP_016866436.1:p.Ile3374=
XM_017010948.2:c.9675C>A	XP_016866437.1:p.Ile3225=
XM_017010949.2:c.8526C>A	XP_016866438.1:p.Ile2842=
XR_001743469.1:n.10662C>A
XR_001744157.1:n.3145+7367G>T
XR_926870.2:n.3145+7367G>T
XR_926871.2:n.3013+7367G>T
XR_926872.2:n.3145+7367G>T
NM_138694.4:c.10386C>A MANE Select	NP_619639.3:p.Ile3462=