Canonical Allele Identifier: CA450613319

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524661A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659863A>G , CM000668.2:g.51659863A>G	GRCh38
NC_000006.11:g.51524661A>G , CM000668.1:g.51524661A>G	GRCh37
NC_000006.10:g.51632620A>G	NCBI36
NG_008753.1:g.432763T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10263T>C MANE Select	ENSP00000360158.3:p.Ile3421=
ENST00000371117.7:c.10263T>C	ENSP00000360158.3:p.Ile3421=
NM_138694.3:c.10263T>C	NP_619639.3:p.Ile3421=
XM_011514679.1:c.10263T>C	XP_011512981.1:p.Ile3421=
XM_011514680.1:c.10263T>C	XP_011512982.1:p.Ile3421=
XM_011514681.1:c.10134T>C	XP_011512983.1:p.Ile3378=
XM_011514682.1:c.10125T>C	XP_011512984.1:p.Ile3375=
XM_011514683.1:c.9621T>C	XP_011512985.1:p.Ile3207=
XM_011514684.1:c.9552T>C	XP_011512986.1:p.Ile3184=
XM_011514687.1:c.10157-10643T>C	XP_011512989.1:n.10157-10643T>C
XM_011514690.1:c.4338T>C	XP_011512992.1:p.Ile1446=
XM_011514691.1:c.4338T>C	XP_011512993.1:p.Ile1446=
XR_926870.1:n.535+7490A>G
XR_926871.1:n.403+7490A>G
XR_926872.1:n.535+7490A>G
XM_011514680.3:c.10263T>C	XP_011512982.1:p.Ile3421=
XM_011514682.3:c.10125T>C	XP_011512984.1:p.Ile3375=
XM_011514683.3:c.9621T>C	XP_011512985.1:p.Ile3207=
XM_011514684.3:c.9552T>C	XP_011512986.1:p.Ile3184=
XM_011514690.3:c.4338T>C	XP_011512992.1:p.Ile1446=
XM_011514691.3:c.4338T>C	XP_011512993.1:p.Ile1446=
XM_017010944.2:c.10263T>C	XP_016866433.1:p.Ile3421=
XM_017010945.2:c.10188T>C	XP_016866434.1:p.Ile3396=
XM_017010946.2:c.10068T>C	XP_016866435.1:p.Ile3356=
XM_017010947.2:c.9999T>C	XP_016866436.1:p.Ile3333=
XM_017010948.2:c.9552T>C	XP_016866437.1:p.Ile3184=
XM_017010949.2:c.8403T>C	XP_016866438.1:p.Ile2801=
XR_001743469.1:n.10539T>C
XR_001744157.1:n.3145+7490A>G
XR_926870.2:n.3145+7490A>G
XR_926871.2:n.3013+7490A>G
XR_926872.2:n.3145+7490A>G
NM_138694.4:c.10263T>C MANE Select	NP_619639.3:p.Ile3421=