Canonical Allele Identifier: CA364436095

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524563C>T (hg19) ; chr6:g.51659765C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659765C>T , CM000668.2:g.51659765C>T	GRCh38
NC_000006.11:g.51524563C>T , CM000668.1:g.51524563C>T	GRCh37
NC_000006.10:g.51632522C>T	NCBI36
NG_008753.1:g.432861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10361G>A MANE Select	ENSP00000360158.3:p.Gly3454Glu
ENST00000371117.7:c.10361G>A	ENSP00000360158.3:p.Gly3454Glu
NM_138694.3:c.10361G>A	NP_619639.3:p.Gly3454Glu
XM_011514679.1:c.10361G>A	XP_011512981.1:p.Gly3454Glu
XM_011514680.1:c.10361G>A	XP_011512982.1:p.Gly3454Glu
XM_011514681.1:c.10232G>A	XP_011512983.1:p.Gly3411Glu
XM_011514682.1:c.10223G>A	XP_011512984.1:p.Gly3408Glu
XM_011514683.1:c.9719G>A	XP_011512985.1:p.Gly3240Glu
XM_011514684.1:c.9650G>A	XP_011512986.1:p.Gly3217Glu
XM_011514687.1:c.10157-10545G>A	XP_011512989.1:n.10157-10545G>A
XM_011514690.1:c.4436G>A	XP_011512992.1:p.Gly1479Glu
XM_011514691.1:c.4436G>A	XP_011512993.1:p.Gly1479Glu
XR_926870.1:n.535+7392C>T
XR_926871.1:n.403+7392C>T
XR_926872.1:n.535+7392C>T
XM_011514680.3:c.10361G>A	XP_011512982.1:p.Gly3454Glu
XM_011514682.3:c.10223G>A	XP_011512984.1:p.Gly3408Glu
XM_011514683.3:c.9719G>A	XP_011512985.1:p.Gly3240Glu
XM_011514684.3:c.9650G>A	XP_011512986.1:p.Gly3217Glu
XM_011514690.3:c.4436G>A	XP_011512992.1:p.Gly1479Glu
XM_011514691.3:c.4436G>A	XP_011512993.1:p.Gly1479Glu
XM_017010944.2:c.10361G>A	XP_016866433.1:p.Gly3454Glu
XM_017010945.2:c.10286G>A	XP_016866434.1:p.Gly3429Glu
XM_017010946.2:c.10166G>A	XP_016866435.1:p.Gly3389Glu
XM_017010947.2:c.10097G>A	XP_016866436.1:p.Gly3366Glu
XM_017010948.2:c.9650G>A	XP_016866437.1:p.Gly3217Glu
XM_017010949.2:c.8501G>A	XP_016866438.1:p.Gly2834Glu
XR_001743469.1:n.10637G>A
XR_001744157.1:n.3145+7392C>T
XR_926870.2:n.3145+7392C>T
XR_926871.2:n.3013+7392C>T
XR_926872.2:n.3145+7392C>T
NM_138694.4:c.10361G>A MANE Select	NP_619639.3:p.Gly3454Glu