Canonical Allele Identifier: CA3851109

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 2794577
• ClinVar RCV Id: RCV003611906
• dbSNP Id: rs746914023
• ExAC: 6:51524619 A / G
• gnomAD v2: 6-51524619-A-G
• gnomAD v3: 6-51659821-A-G
• gnomAD v4: 6-51659821-A-G
• MyVariant Identifiers: chr6:g.51524619A>G (hg19) ; chr6:g.51659821A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659821A>G , CM000668.2:g.51659821A>G	GRCh38
NC_000006.11:g.51524619A>G , CM000668.1:g.51524619A>G	GRCh37
NC_000006.10:g.51632578A>G	NCBI36
NG_008753.1:g.432805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10305T>C MANE Select	ENSP00000360158.3:p.Ser3435=
ENST00000371117.7:c.10305T>C	ENSP00000360158.3:p.Ser3435=
NM_138694.3:c.10305T>C	NP_619639.3:p.Ser3435=
XM_011514679.1:c.10305T>C	XP_011512981.1:p.Ser3435=
XM_011514680.1:c.10305T>C	XP_011512982.1:p.Ser3435=
XM_011514681.1:c.10176T>C	XP_011512983.1:p.Ser3392=
XM_011514682.1:c.10167T>C	XP_011512984.1:p.Ser3389=
XM_011514683.1:c.9663T>C	XP_011512985.1:p.Ser3221=
XM_011514684.1:c.9594T>C	XP_011512986.1:p.Ser3198=
XM_011514687.1:c.10157-10601T>C	XP_011512989.1:n.10157-10601T>C
XM_011514690.1:c.4380T>C	XP_011512992.1:p.Ser1460=
XM_011514691.1:c.4380T>C	XP_011512993.1:p.Ser1460=
XR_926870.1:n.535+7448A>G
XR_926871.1:n.403+7448A>G
XR_926872.1:n.535+7448A>G
XM_011514680.3:c.10305T>C	XP_011512982.1:p.Ser3435=
XM_011514682.3:c.10167T>C	XP_011512984.1:p.Ser3389=
XM_011514683.3:c.9663T>C	XP_011512985.1:p.Ser3221=
XM_011514684.3:c.9594T>C	XP_011512986.1:p.Ser3198=
XM_011514690.3:c.4380T>C	XP_011512992.1:p.Ser1460=
XM_011514691.3:c.4380T>C	XP_011512993.1:p.Ser1460=
XM_017010944.2:c.10305T>C	XP_016866433.1:p.Ser3435=
XM_017010945.2:c.10230T>C	XP_016866434.1:p.Ser3410=
XM_017010946.2:c.10110T>C	XP_016866435.1:p.Ser3370=
XM_017010947.2:c.10041T>C	XP_016866436.1:p.Ser3347=
XM_017010948.2:c.9594T>C	XP_016866437.1:p.Ser3198=
XM_017010949.2:c.8445T>C	XP_016866438.1:p.Ser2815=
XR_001743469.1:n.10581T>C
XR_001744157.1:n.3145+7448A>G
XR_926870.2:n.3145+7448A>G
XR_926871.2:n.3013+7448A>G
XR_926872.2:n.3145+7448A>G
NM_138694.4:c.10305T>C MANE Select	NP_619639.3:p.Ser3435=