Canonical Allele Identifier: CA364436494

Gene: PKHD1

Linked Data

• COSMIC: COSM4519846
• MyVariant Identifiers: chr6:g.51524618C>T (hg19) ; chr6:g.51659820C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659820C>T , CM000668.2:g.51659820C>T	GRCh38
NC_000006.11:g.51524618C>T , CM000668.1:g.51524618C>T	GRCh37
NC_000006.10:g.51632577C>T	NCBI36
NG_008753.1:g.432806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10306G>A MANE Select	ENSP00000360158.3:p.Gly3436Ser
ENST00000371117.7:c.10306G>A	ENSP00000360158.3:p.Gly3436Ser
NM_138694.3:c.10306G>A	NP_619639.3:p.Gly3436Ser
XM_011514679.1:c.10306G>A	XP_011512981.1:p.Gly3436Ser
XM_011514680.1:c.10306G>A	XP_011512982.1:p.Gly3436Ser
XM_011514681.1:c.10177G>A	XP_011512983.1:p.Gly3393Ser
XM_011514682.1:c.10168G>A	XP_011512984.1:p.Gly3390Ser
XM_011514683.1:c.9664G>A	XP_011512985.1:p.Gly3222Ser
XM_011514684.1:c.9595G>A	XP_011512986.1:p.Gly3199Ser
XM_011514687.1:c.10157-10600G>A	XP_011512989.1:n.10157-10600G>A
XM_011514690.1:c.4381G>A	XP_011512992.1:p.Gly1461Ser
XM_011514691.1:c.4381G>A	XP_011512993.1:p.Gly1461Ser
XR_926870.1:n.535+7447C>T
XR_926871.1:n.403+7447C>T
XR_926872.1:n.535+7447C>T
XM_011514680.3:c.10306G>A	XP_011512982.1:p.Gly3436Ser
XM_011514682.3:c.10168G>A	XP_011512984.1:p.Gly3390Ser
XM_011514683.3:c.9664G>A	XP_011512985.1:p.Gly3222Ser
XM_011514684.3:c.9595G>A	XP_011512986.1:p.Gly3199Ser
XM_011514690.3:c.4381G>A	XP_011512992.1:p.Gly1461Ser
XM_011514691.3:c.4381G>A	XP_011512993.1:p.Gly1461Ser
XM_017010944.2:c.10306G>A	XP_016866433.1:p.Gly3436Ser
XM_017010945.2:c.10231G>A	XP_016866434.1:p.Gly3411Ser
XM_017010946.2:c.10111G>A	XP_016866435.1:p.Gly3371Ser
XM_017010947.2:c.10042G>A	XP_016866436.1:p.Gly3348Ser
XM_017010948.2:c.9595G>A	XP_016866437.1:p.Gly3199Ser
XM_017010949.2:c.8446G>A	XP_016866438.1:p.Gly2816Ser
XR_001743469.1:n.10582G>A
XR_001744157.1:n.3145+7447C>T
XR_926870.2:n.3145+7447C>T
XR_926871.2:n.3013+7447C>T
XR_926872.2:n.3145+7447C>T
NM_138694.4:c.10306G>A MANE Select	NP_619639.3:p.Gly3436Ser