Canonical Allele Identifier: CA364418970

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491901T>A (hg19) ; chr6:g.51627103T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627103T>A , CM000668.2:g.51627103T>A	GRCh38
NC_000006.11:g.51491901T>A , CM000668.1:g.51491901T>A	GRCh37
NC_000006.10:g.51599860T>A	NCBI36
NG_008753.1:g.465523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11679A>T MANE Select	ENSP00000360158.3:p.Glu3893Asp
ENST00000371117.7:c.11679A>T	ENSP00000360158.3:p.Glu3893Asp
NM_138694.3:c.11679A>T	NP_619639.3:p.Glu3893Asp
XM_011514679.1:c.11679A>T	XP_011512981.1:p.Glu3893Asp
XM_011514680.1:c.11679A>T	XP_011512982.1:p.Glu3893Asp
XM_011514681.1:c.11550A>T	XP_011512983.1:p.Glu3850Asp
XM_011514682.1:c.11541A>T	XP_011512984.1:p.Glu3847Asp
XM_011514683.1:c.11037A>T	XP_011512985.1:p.Glu3679Asp
XM_011514684.1:c.10968A>T	XP_011512986.1:p.Glu3656Asp
XM_011514690.1:c.5754A>T	XP_011512992.1:p.Glu1918Asp
XM_011514691.1:c.5754A>T	XP_011512993.1:p.Glu1918Asp
XM_011514680.3:c.11679A>T	XP_011512982.1:p.Glu3893Asp
XM_011514682.3:c.11541A>T	XP_011512984.1:p.Glu3847Asp
XM_011514683.3:c.11037A>T	XP_011512985.1:p.Glu3679Asp
XM_011514684.3:c.10968A>T	XP_011512986.1:p.Glu3656Asp
XM_011514690.3:c.5754A>T	XP_011512992.1:p.Glu1918Asp
XM_011514691.3:c.5754A>T	XP_011512993.1:p.Glu1918Asp
XM_017010944.2:c.11679A>T	XP_016866433.1:p.Glu3893Asp
XM_017010945.2:c.11604A>T	XP_016866434.1:p.Glu3868Asp
XM_017010946.2:c.11484A>T	XP_016866435.1:p.Glu3828Asp
XM_017010947.2:c.11415A>T	XP_016866436.1:p.Glu3805Asp
XM_017010948.2:c.10968A>T	XP_016866437.1:p.Glu3656Asp
XM_017010949.2:c.9819A>T	XP_016866438.1:p.Glu3273Asp
NM_138694.4:c.11679A>T MANE Select	NP_619639.3:p.Glu3893Asp