Canonical Allele Identifier: CA364431173

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51523996T>A (hg19) ; chr6:g.51659198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659198T>A , CM000668.2:g.51659198T>A	GRCh38
NC_000006.11:g.51523996T>A , CM000668.1:g.51523996T>A	GRCh37
NC_000006.10:g.51631955T>A	NCBI36
NG_008753.1:g.433428A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10928A>T MANE Select	ENSP00000360158.3:p.Glu3643Val
ENST00000371117.7:c.10928A>T	ENSP00000360158.3:p.Glu3643Val
NM_138694.3:c.10928A>T	NP_619639.3:p.Glu3643Val
XM_011514679.1:c.10928A>T	XP_011512981.1:p.Glu3643Val
XM_011514680.1:c.10928A>T	XP_011512982.1:p.Glu3643Val
XM_011514681.1:c.10799A>T	XP_011512983.1:p.Glu3600Val
XM_011514682.1:c.10790A>T	XP_011512984.1:p.Glu3597Val
XM_011514683.1:c.10286A>T	XP_011512985.1:p.Glu3429Val
XM_011514684.1:c.10217A>T	XP_011512986.1:p.Glu3406Val
XM_011514687.1:c.10157-9978A>T	XP_011512989.1:n.10157-9978A>T
XM_011514690.1:c.5003A>T	XP_011512992.1:p.Glu1668Val
XM_011514691.1:c.5003A>T	XP_011512993.1:p.Glu1668Val
XR_926870.1:n.535+6825T>A
XR_926871.1:n.403+6825T>A
XR_926872.1:n.535+6825T>A
XM_011514680.3:c.10928A>T	XP_011512982.1:p.Glu3643Val
XM_011514682.3:c.10790A>T	XP_011512984.1:p.Glu3597Val
XM_011514683.3:c.10286A>T	XP_011512985.1:p.Glu3429Val
XM_011514684.3:c.10217A>T	XP_011512986.1:p.Glu3406Val
XM_011514690.3:c.5003A>T	XP_011512992.1:p.Glu1668Val
XM_011514691.3:c.5003A>T	XP_011512993.1:p.Glu1668Val
XM_017010944.2:c.10928A>T	XP_016866433.1:p.Glu3643Val
XM_017010945.2:c.10853A>T	XP_016866434.1:p.Glu3618Val
XM_017010946.2:c.10733A>T	XP_016866435.1:p.Glu3578Val
XM_017010947.2:c.10664A>T	XP_016866436.1:p.Glu3555Val
XM_017010948.2:c.10217A>T	XP_016866437.1:p.Glu3406Val
XM_017010949.2:c.9068A>T	XP_016866438.1:p.Glu3023Val
XR_001743469.1:n.11204A>T
XR_001744157.1:n.3145+6825T>A
XR_926870.2:n.3145+6825T>A
XR_926871.2:n.3013+6825T>A
XR_926872.2:n.3145+6825T>A
NM_138694.4:c.10928A>T MANE Select	NP_619639.3:p.Glu3643Val