Canonical Allele Identifier: CA364421395

Gene: PKHD1

Linked Data

• gnomAD v4: 6-51748274-A-C
• MyVariant Identifiers: chr6:g.51613072A>C (hg19) ; chr6:g.51748274A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748274A>C , CM000668.2:g.51748274A>C	GRCh38
NC_000006.11:g.51613072A>C , CM000668.1:g.51613072A>C	GRCh37
NC_000006.10:g.51721031A>C	NCBI36
NG_008753.1:g.344352T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9342T>G MANE Select	ENSP00000360158.3:p.Cys3114Trp
ENST00000340994.4:c.9342T>G	ENSP00000341097.4:p.Cys3114Trp
ENST00000371117.7:c.9342T>G	ENSP00000360158.3:p.Cys3114Trp
NM_138694.3:c.9342T>G	NP_619639.3:p.Cys3114Trp
NM_170724.2:c.9342T>G	NP_733842.2:p.Cys3114Trp
XM_011514679.1:c.9342T>G	XP_011512981.1:p.Cys3114Trp
XM_011514680.1:c.9342T>G	XP_011512982.1:p.Cys3114Trp
XM_011514681.1:c.9213T>G	XP_011512983.1:p.Cys3071Trp
XM_011514682.1:c.9204T>G	XP_011512984.1:p.Cys3068Trp
XM_011514683.1:c.8700T>G	XP_011512985.1:p.Cys2900Trp
XM_011514684.1:c.8631T>G	XP_011512986.1:p.Cys2877Trp
XM_011514685.1:c.9342T>G	XP_011512987.1:p.Cys3114Trp
XM_011514686.1:c.9342T>G	XP_011512988.1:p.Cys3114Trp
XM_011514687.1:c.9342T>G	XP_011512989.1:p.Cys3114Trp
XM_011514688.1:c.9342T>G	XP_011512990.1:p.Cys3114Trp
XM_011514690.1:c.3417T>G	XP_011512992.1:p.Cys1139Trp
XM_011514691.1:c.3417T>G	XP_011512993.1:p.Cys1139Trp
XM_011514680.3:c.9342T>G	XP_011512982.1:p.Cys3114Trp
XM_011514682.3:c.9204T>G	XP_011512984.1:p.Cys3068Trp
XM_011514683.3:c.8700T>G	XP_011512985.1:p.Cys2900Trp
XM_011514684.3:c.8631T>G	XP_011512986.1:p.Cys2877Trp
XM_011514686.2:c.9342T>G	XP_011512988.1:p.Cys3114Trp
XM_011514688.2:c.9342T>G	XP_011512990.1:p.Cys3114Trp
XM_011514690.3:c.3417T>G	XP_011512992.1:p.Cys1139Trp
XM_011514691.3:c.3417T>G	XP_011512993.1:p.Cys1139Trp
XM_017010944.2:c.9342T>G	XP_016866433.1:p.Cys3114Trp
XM_017010945.2:c.9267T>G	XP_016866434.1:p.Cys3089Trp
XM_017010946.2:c.9147T>G	XP_016866435.1:p.Cys3049Trp
XM_017010947.2:c.9078T>G	XP_016866436.1:p.Cys3026Trp
XM_017010948.2:c.8631T>G	XP_016866437.1:p.Cys2877Trp
XM_017010949.2:c.7482T>G	XP_016866438.1:p.Cys2494Trp
XM_017010950.1:c.9342T>G	XP_016866439.1:p.Cys3114Trp
XR_001743469.1:n.9618T>G
NM_138694.4:c.9342T>G MANE Select	NP_619639.3:p.Cys3114Trp
NM_170724.3:c.9342T>G	NP_733842.2:p.Cys3114Trp