Canonical Allele Identifier: CA364437673

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524758C>G (hg19) ; chr6:g.51659960C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659960C>G , CM000668.2:g.51659960C>G	GRCh38
NC_000006.11:g.51524758C>G , CM000668.1:g.51524758C>G	GRCh37
NC_000006.10:g.51632717C>G	NCBI36
NG_008753.1:g.432666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10166G>C MANE Select	ENSP00000360158.3:p.Arg3389Thr
ENST00000371117.7:c.10166G>C	ENSP00000360158.3:p.Arg3389Thr
NM_138694.3:c.10166G>C	NP_619639.3:p.Arg3389Thr
XM_011514679.1:c.10166G>C	XP_011512981.1:p.Arg3389Thr
XM_011514680.1:c.10166G>C	XP_011512982.1:p.Arg3389Thr
XM_011514681.1:c.10037G>C	XP_011512983.1:p.Arg3346Thr
XM_011514682.1:c.10028G>C	XP_011512984.1:p.Arg3343Thr
XM_011514683.1:c.9524G>C	XP_011512985.1:p.Arg3175Thr
XM_011514684.1:c.9455G>C	XP_011512986.1:p.Arg3152Thr
XM_011514687.1:c.10157-10740G>C	XP_011512989.1:n.10157-10740G>C
XM_011514690.1:c.4241G>C	XP_011512992.1:p.Arg1414Thr
XM_011514691.1:c.4241G>C	XP_011512993.1:p.Arg1414Thr
XR_926870.1:n.535+7587C>G
XR_926871.1:n.403+7587C>G
XR_926872.1:n.535+7587C>G
XM_011514680.3:c.10166G>C	XP_011512982.1:p.Arg3389Thr
XM_011514682.3:c.10028G>C	XP_011512984.1:p.Arg3343Thr
XM_011514683.3:c.9524G>C	XP_011512985.1:p.Arg3175Thr
XM_011514684.3:c.9455G>C	XP_011512986.1:p.Arg3152Thr
XM_011514690.3:c.4241G>C	XP_011512992.1:p.Arg1414Thr
XM_011514691.3:c.4241G>C	XP_011512993.1:p.Arg1414Thr
XM_017010944.2:c.10166G>C	XP_016866433.1:p.Arg3389Thr
XM_017010945.2:c.10091G>C	XP_016866434.1:p.Arg3364Thr
XM_017010946.2:c.9971G>C	XP_016866435.1:p.Arg3324Thr
XM_017010947.2:c.9902G>C	XP_016866436.1:p.Arg3301Thr
XM_017010948.2:c.9455G>C	XP_016866437.1:p.Arg3152Thr
XM_017010949.2:c.8306G>C	XP_016866438.1:p.Arg2769Thr
XR_001743469.1:n.10442G>C
XR_001744157.1:n.3145+7587C>G
XR_926870.2:n.3145+7587C>G
XR_926871.2:n.3013+7587C>G
XR_926872.2:n.3145+7587C>G
NM_138694.4:c.10166G>C MANE Select	NP_619639.3:p.Arg3389Thr