Canonical Allele Identifier: CA364429778

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51523768T>A (hg19) ; chr6:g.51658970T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51658970T>A , CM000668.2:g.51658970T>A	GRCh38
NC_000006.11:g.51523768T>A , CM000668.1:g.51523768T>A	GRCh37
NC_000006.10:g.51631727T>A	NCBI36
NG_008753.1:g.433656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11156A>T MANE Select	ENSP00000360158.3:p.Lys3719Met
ENST00000371117.7:c.11156A>T	ENSP00000360158.3:p.Lys3719Met
NM_138694.3:c.11156A>T	NP_619639.3:p.Lys3719Met
XM_011514679.1:c.11156A>T	XP_011512981.1:p.Lys3719Met
XM_011514680.1:c.11156A>T	XP_011512982.1:p.Lys3719Met
XM_011514681.1:c.11027A>T	XP_011512983.1:p.Lys3676Met
XM_011514682.1:c.11018A>T	XP_011512984.1:p.Lys3673Met
XM_011514683.1:c.10514A>T	XP_011512985.1:p.Lys3505Met
XM_011514684.1:c.10445A>T	XP_011512986.1:p.Lys3482Met
XM_011514687.1:c.10157-9750A>T	XP_011512989.1:n.10157-9750A>T
XM_011514690.1:c.5231A>T	XP_011512992.1:p.Lys1744Met
XM_011514691.1:c.5231A>T	XP_011512993.1:p.Lys1744Met
XR_926870.1:n.535+6597T>A
XR_926871.1:n.403+6597T>A
XR_926872.1:n.535+6597T>A
XM_011514680.3:c.11156A>T	XP_011512982.1:p.Lys3719Met
XM_011514682.3:c.11018A>T	XP_011512984.1:p.Lys3673Met
XM_011514683.3:c.10514A>T	XP_011512985.1:p.Lys3505Met
XM_011514684.3:c.10445A>T	XP_011512986.1:p.Lys3482Met
XM_011514690.3:c.5231A>T	XP_011512992.1:p.Lys1744Met
XM_011514691.3:c.5231A>T	XP_011512993.1:p.Lys1744Met
XM_017010944.2:c.11156A>T	XP_016866433.1:p.Lys3719Met
XM_017010945.2:c.11081A>T	XP_016866434.1:p.Lys3694Met
XM_017010946.2:c.10961A>T	XP_016866435.1:p.Lys3654Met
XM_017010947.2:c.10892A>T	XP_016866436.1:p.Lys3631Met
XM_017010948.2:c.10445A>T	XP_016866437.1:p.Lys3482Met
XM_017010949.2:c.9296A>T	XP_016866438.1:p.Lys3099Met
XR_001743469.1:n.11432A>T
XR_001744157.1:n.3145+6597T>A
XR_926870.2:n.3145+6597T>A
XR_926871.2:n.3013+6597T>A
XR_926872.2:n.3145+6597T>A
NM_138694.4:c.11156A>T MANE Select	NP_619639.3:p.Lys3719Met