Canonical Allele Identifier: CA364434417

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524401A>T (hg19) ; chr6:g.51659603A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659603A>T , CM000668.2:g.51659603A>T	GRCh38
NC_000006.11:g.51524401A>T , CM000668.1:g.51524401A>T	GRCh37
NC_000006.10:g.51632360A>T	NCBI36
NG_008753.1:g.433023T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10523T>A MANE Select	ENSP00000360158.3:p.Val3508Asp
ENST00000371117.7:c.10523T>A	ENSP00000360158.3:p.Val3508Asp
NM_138694.3:c.10523T>A	NP_619639.3:p.Val3508Asp
XM_011514679.1:c.10523T>A	XP_011512981.1:p.Val3508Asp
XM_011514680.1:c.10523T>A	XP_011512982.1:p.Val3508Asp
XM_011514681.1:c.10394T>A	XP_011512983.1:p.Val3465Asp
XM_011514682.1:c.10385T>A	XP_011512984.1:p.Val3462Asp
XM_011514683.1:c.9881T>A	XP_011512985.1:p.Val3294Asp
XM_011514684.1:c.9812T>A	XP_011512986.1:p.Val3271Asp
XM_011514687.1:c.10157-10383T>A	XP_011512989.1:n.10157-10383T>A
XM_011514690.1:c.4598T>A	XP_011512992.1:p.Val1533Asp
XM_011514691.1:c.4598T>A	XP_011512993.1:p.Val1533Asp
XR_926870.1:n.535+7230A>T
XR_926871.1:n.403+7230A>T
XR_926872.1:n.535+7230A>T
XM_011514680.3:c.10523T>A	XP_011512982.1:p.Val3508Asp
XM_011514682.3:c.10385T>A	XP_011512984.1:p.Val3462Asp
XM_011514683.3:c.9881T>A	XP_011512985.1:p.Val3294Asp
XM_011514684.3:c.9812T>A	XP_011512986.1:p.Val3271Asp
XM_011514690.3:c.4598T>A	XP_011512992.1:p.Val1533Asp
XM_011514691.3:c.4598T>A	XP_011512993.1:p.Val1533Asp
XM_017010944.2:c.10523T>A	XP_016866433.1:p.Val3508Asp
XM_017010945.2:c.10448T>A	XP_016866434.1:p.Val3483Asp
XM_017010946.2:c.10328T>A	XP_016866435.1:p.Val3443Asp
XM_017010947.2:c.10259T>A	XP_016866436.1:p.Val3420Asp
XM_017010948.2:c.9812T>A	XP_016866437.1:p.Val3271Asp
XM_017010949.2:c.8663T>A	XP_016866438.1:p.Val2888Asp
XR_001743469.1:n.10799T>A
XR_001744157.1:n.3145+7230A>T
XR_926870.2:n.3145+7230A>T
XR_926871.2:n.3013+7230A>T
XR_926872.2:n.3145+7230A>T
NM_138694.4:c.10523T>A MANE Select	NP_619639.3:p.Val3508Asp