Canonical Allele Identifier: CA450613242

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 1122565
• ClinVar RCV Id: RCV001453241
• dbSNP Id: rs1466831280
• gnomAD v2: 6-51524468-A-G
• gnomAD v4: 6-51659670-A-G
• MyVariant Identifiers: chr6:g.51524468A>G (hg19) ; chr6:g.51659670A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659670A>G , CM000668.2:g.51659670A>G	GRCh38
NC_000006.11:g.51524468A>G , CM000668.1:g.51524468A>G	GRCh37
NC_000006.10:g.51632427A>G	NCBI36
NG_008753.1:g.432956T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10456T>C MANE Select	ENSP00000360158.3:p.Leu3486=
ENST00000371117.7:c.10456T>C	ENSP00000360158.3:p.Leu3486=
NM_138694.3:c.10456T>C	NP_619639.3:p.Leu3486=
XM_011514679.1:c.10456T>C	XP_011512981.1:p.Leu3486=
XM_011514680.1:c.10456T>C	XP_011512982.1:p.Leu3486=
XM_011514681.1:c.10327T>C	XP_011512983.1:p.Leu3443=
XM_011514682.1:c.10318T>C	XP_011512984.1:p.Leu3440=
XM_011514683.1:c.9814T>C	XP_011512985.1:p.Leu3272=
XM_011514684.1:c.9745T>C	XP_011512986.1:p.Leu3249=
XM_011514687.1:c.10157-10450T>C	XP_011512989.1:n.10157-10450T>C
XM_011514690.1:c.4531T>C	XP_011512992.1:p.Leu1511=
XM_011514691.1:c.4531T>C	XP_011512993.1:p.Leu1511=
XR_926870.1:n.535+7297A>G
XR_926871.1:n.403+7297A>G
XR_926872.1:n.535+7297A>G
XM_011514680.3:c.10456T>C	XP_011512982.1:p.Leu3486=
XM_011514682.3:c.10318T>C	XP_011512984.1:p.Leu3440=
XM_011514683.3:c.9814T>C	XP_011512985.1:p.Leu3272=
XM_011514684.3:c.9745T>C	XP_011512986.1:p.Leu3249=
XM_011514690.3:c.4531T>C	XP_011512992.1:p.Leu1511=
XM_011514691.3:c.4531T>C	XP_011512993.1:p.Leu1511=
XM_017010944.2:c.10456T>C	XP_016866433.1:p.Leu3486=
XM_017010945.2:c.10381T>C	XP_016866434.1:p.Leu3461=
XM_017010946.2:c.10261T>C	XP_016866435.1:p.Leu3421=
XM_017010947.2:c.10192T>C	XP_016866436.1:p.Leu3398=
XM_017010948.2:c.9745T>C	XP_016866437.1:p.Leu3249=
XM_017010949.2:c.8596T>C	XP_016866438.1:p.Leu2866=
XR_001743469.1:n.10732T>C
XR_001744157.1:n.3145+7297A>G
XR_926870.2:n.3145+7297A>G
XR_926871.2:n.3013+7297A>G
XR_926872.2:n.3145+7297A>G
NM_138694.4:c.10456T>C MANE Select	NP_619639.3:p.Leu3486=