Canonical Allele Identifier: CA3851103

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 1082974
• ClinVar RCV Id: RCV001399497
• dbSNP Id: rs368317856
• ExAC: 6:51524604 G / A
• gnomAD v2: 6-51524604-G-A
• gnomAD v3: 6-51659806-G-A
• gnomAD v4: 6-51659806-G-A
• MyVariant Identifiers: chr6:g.51524604G>A (hg19) ; chr6:g.51659806G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659806G>A , CM000668.2:g.51659806G>A	GRCh38
NC_000006.11:g.51524604G>A , CM000668.1:g.51524604G>A	GRCh37
NC_000006.10:g.51632563G>A	NCBI36
NG_008753.1:g.432820C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10320C>T MANE Select	ENSP00000360158.3:p.Val3440=
ENST00000371117.7:c.10320C>T	ENSP00000360158.3:p.Val3440=
NM_138694.3:c.10320C>T	NP_619639.3:p.Val3440=
XM_011514679.1:c.10320C>T	XP_011512981.1:p.Val3440=
XM_011514680.1:c.10320C>T	XP_011512982.1:p.Val3440=
XM_011514681.1:c.10191C>T	XP_011512983.1:p.Val3397=
XM_011514682.1:c.10182C>T	XP_011512984.1:p.Val3394=
XM_011514683.1:c.9678C>T	XP_011512985.1:p.Val3226=
XM_011514684.1:c.9609C>T	XP_011512986.1:p.Val3203=
XM_011514687.1:c.10157-10586C>T	XP_011512989.1:n.10157-10586C>T
XM_011514690.1:c.4395C>T	XP_011512992.1:p.Val1465=
XM_011514691.1:c.4395C>T	XP_011512993.1:p.Val1465=
XR_926870.1:n.535+7433G>A
XR_926871.1:n.403+7433G>A
XR_926872.1:n.535+7433G>A
XM_011514680.3:c.10320C>T	XP_011512982.1:p.Val3440=
XM_011514682.3:c.10182C>T	XP_011512984.1:p.Val3394=
XM_011514683.3:c.9678C>T	XP_011512985.1:p.Val3226=
XM_011514684.3:c.9609C>T	XP_011512986.1:p.Val3203=
XM_011514690.3:c.4395C>T	XP_011512992.1:p.Val1465=
XM_011514691.3:c.4395C>T	XP_011512993.1:p.Val1465=
XM_017010944.2:c.10320C>T	XP_016866433.1:p.Val3440=
XM_017010945.2:c.10245C>T	XP_016866434.1:p.Val3415=
XM_017010946.2:c.10125C>T	XP_016866435.1:p.Val3375=
XM_017010947.2:c.10056C>T	XP_016866436.1:p.Val3352=
XM_017010948.2:c.9609C>T	XP_016866437.1:p.Val3203=
XM_017010949.2:c.8460C>T	XP_016866438.1:p.Val2820=
XR_001743469.1:n.10596C>T
XR_001744157.1:n.3145+7433G>A
XR_926870.2:n.3145+7433G>A
XR_926871.2:n.3013+7433G>A
XR_926872.2:n.3145+7433G>A
NM_138694.4:c.10320C>T MANE Select	NP_619639.3:p.Val3440=