Canonical Allele Identifier: CA364431000

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51523970G>T (hg19) ; chr6:g.51659172G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659172G>T , CM000668.2:g.51659172G>T	GRCh38
NC_000006.11:g.51523970G>T , CM000668.1:g.51523970G>T	GRCh37
NC_000006.10:g.51631929G>T	NCBI36
NG_008753.1:g.433454C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10954C>A MANE Select	ENSP00000360158.3:p.Pro3652Thr
ENST00000371117.7:c.10954C>A	ENSP00000360158.3:p.Pro3652Thr
NM_138694.3:c.10954C>A	NP_619639.3:p.Pro3652Thr
XM_011514679.1:c.10954C>A	XP_011512981.1:p.Pro3652Thr
XM_011514680.1:c.10954C>A	XP_011512982.1:p.Pro3652Thr
XM_011514681.1:c.10825C>A	XP_011512983.1:p.Pro3609Thr
XM_011514682.1:c.10816C>A	XP_011512984.1:p.Pro3606Thr
XM_011514683.1:c.10312C>A	XP_011512985.1:p.Pro3438Thr
XM_011514684.1:c.10243C>A	XP_011512986.1:p.Pro3415Thr
XM_011514687.1:c.10157-9952C>A	XP_011512989.1:n.10157-9952C>A
XM_011514690.1:c.5029C>A	XP_011512992.1:p.Pro1677Thr
XM_011514691.1:c.5029C>A	XP_011512993.1:p.Pro1677Thr
XR_926870.1:n.535+6799G>T
XR_926871.1:n.403+6799G>T
XR_926872.1:n.535+6799G>T
XM_011514680.3:c.10954C>A	XP_011512982.1:p.Pro3652Thr
XM_011514682.3:c.10816C>A	XP_011512984.1:p.Pro3606Thr
XM_011514683.3:c.10312C>A	XP_011512985.1:p.Pro3438Thr
XM_011514684.3:c.10243C>A	XP_011512986.1:p.Pro3415Thr
XM_011514690.3:c.5029C>A	XP_011512992.1:p.Pro1677Thr
XM_011514691.3:c.5029C>A	XP_011512993.1:p.Pro1677Thr
XM_017010944.2:c.10954C>A	XP_016866433.1:p.Pro3652Thr
XM_017010945.2:c.10879C>A	XP_016866434.1:p.Pro3627Thr
XM_017010946.2:c.10759C>A	XP_016866435.1:p.Pro3587Thr
XM_017010947.2:c.10690C>A	XP_016866436.1:p.Pro3564Thr
XM_017010948.2:c.10243C>A	XP_016866437.1:p.Pro3415Thr
XM_017010949.2:c.9094C>A	XP_016866438.1:p.Pro3032Thr
XR_001743469.1:n.11230C>A
XR_001744157.1:n.3145+6799G>T
XR_926870.2:n.3145+6799G>T
XR_926871.2:n.3013+6799G>T
XR_926872.2:n.3145+6799G>T
NM_138694.4:c.10954C>A MANE Select	NP_619639.3:p.Pro3652Thr