Canonical Allele Identifier: CA364431119

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51523989G>T (hg19) ; chr6:g.51659191G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659191G>T , CM000668.2:g.51659191G>T	GRCh38
NC_000006.11:g.51523989G>T , CM000668.1:g.51523989G>T	GRCh37
NC_000006.10:g.51631948G>T	NCBI36
NG_008753.1:g.433435C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10935C>A MANE Select	ENSP00000360158.3:p.Asn3645Lys
ENST00000371117.7:c.10935C>A	ENSP00000360158.3:p.Asn3645Lys
NM_138694.3:c.10935C>A	NP_619639.3:p.Asn3645Lys
XM_011514679.1:c.10935C>A	XP_011512981.1:p.Asn3645Lys
XM_011514680.1:c.10935C>A	XP_011512982.1:p.Asn3645Lys
XM_011514681.1:c.10806C>A	XP_011512983.1:p.Asn3602Lys
XM_011514682.1:c.10797C>A	XP_011512984.1:p.Asn3599Lys
XM_011514683.1:c.10293C>A	XP_011512985.1:p.Asn3431Lys
XM_011514684.1:c.10224C>A	XP_011512986.1:p.Asn3408Lys
XM_011514687.1:c.10157-9971C>A	XP_011512989.1:n.10157-9971C>A
XM_011514690.1:c.5010C>A	XP_011512992.1:p.Asn1670Lys
XM_011514691.1:c.5010C>A	XP_011512993.1:p.Asn1670Lys
XR_926870.1:n.535+6818G>T
XR_926871.1:n.403+6818G>T
XR_926872.1:n.535+6818G>T
XM_011514680.3:c.10935C>A	XP_011512982.1:p.Asn3645Lys
XM_011514682.3:c.10797C>A	XP_011512984.1:p.Asn3599Lys
XM_011514683.3:c.10293C>A	XP_011512985.1:p.Asn3431Lys
XM_011514684.3:c.10224C>A	XP_011512986.1:p.Asn3408Lys
XM_011514690.3:c.5010C>A	XP_011512992.1:p.Asn1670Lys
XM_011514691.3:c.5010C>A	XP_011512993.1:p.Asn1670Lys
XM_017010944.2:c.10935C>A	XP_016866433.1:p.Asn3645Lys
XM_017010945.2:c.10860C>A	XP_016866434.1:p.Asn3620Lys
XM_017010946.2:c.10740C>A	XP_016866435.1:p.Asn3580Lys
XM_017010947.2:c.10671C>A	XP_016866436.1:p.Asn3557Lys
XM_017010948.2:c.10224C>A	XP_016866437.1:p.Asn3408Lys
XM_017010949.2:c.9075C>A	XP_016866438.1:p.Asn3025Lys
XR_001743469.1:n.11211C>A
XR_001744157.1:n.3145+6818G>T
XR_926870.2:n.3145+6818G>T
XR_926871.2:n.3013+6818G>T
XR_926872.2:n.3145+6818G>T
NM_138694.4:c.10935C>A MANE Select	NP_619639.3:p.Asn3645Lys