Canonical Allele Identifier: CA450412706

Gene: PKHD1

Linked Data

• dbSNP Id: rs2151012018
• MyVariant Identifiers: chr6:g.51618123T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51753325T>C , CM000668.2:g.51753325T>C	GRCh38
NC_000006.11:g.51618123T>C , CM000668.1:g.51618123T>C	GRCh37
NC_000006.10:g.51726082T>C	NCBI36
NG_008753.1:g.339301A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.8826A>G MANE Select	ENSP00000360158.3:p.Arg2942=
ENST00000340994.4:c.8826A>G	ENSP00000341097.4:p.Arg2942=
ENST00000371117.7:c.8826A>G	ENSP00000360158.3:p.Arg2942=
NM_138694.3:c.8826A>G	NP_619639.3:p.Arg2942=
NM_170724.2:c.8826A>G	NP_733842.2:p.Arg2942=
XM_011514679.1:c.8826A>G	XP_011512981.1:p.Arg2942=
XM_011514680.1:c.8826A>G	XP_011512982.1:p.Arg2942=
XM_011514681.1:c.8697A>G	XP_011512983.1:p.Arg2899=
XM_011514682.1:c.8688A>G	XP_011512984.1:p.Arg2896=
XM_011514683.1:c.8184A>G	XP_011512985.1:p.Arg2728=
XM_011514684.1:c.8115A>G	XP_011512986.1:p.Arg2705=
XM_011514685.1:c.8826A>G	XP_011512987.1:p.Arg2942=
XM_011514686.1:c.8826A>G	XP_011512988.1:p.Arg2942=
XM_011514687.1:c.8826A>G	XP_011512989.1:p.Arg2942=
XM_011514688.1:c.8826A>G	XP_011512990.1:p.Arg2942=
XM_011514690.1:c.2901A>G	XP_011512992.1:p.Arg967=
XM_011514691.1:c.2901A>G	XP_011512993.1:p.Arg967=
XM_011514680.3:c.8826A>G	XP_011512982.1:p.Arg2942=
XM_011514682.3:c.8688A>G	XP_011512984.1:p.Arg2896=
XM_011514683.3:c.8184A>G	XP_011512985.1:p.Arg2728=
XM_011514684.3:c.8115A>G	XP_011512986.1:p.Arg2705=
XM_011514686.2:c.8826A>G	XP_011512988.1:p.Arg2942=
XM_011514688.2:c.8826A>G	XP_011512990.1:p.Arg2942=
XM_011514690.3:c.2901A>G	XP_011512992.1:p.Arg967=
XM_011514691.3:c.2901A>G	XP_011512993.1:p.Arg967=
XM_017010944.2:c.8826A>G	XP_016866433.1:p.Arg2942=
XM_017010945.2:c.8751A>G	XP_016866434.1:p.Arg2917=
XM_017010946.2:c.8631A>G	XP_016866435.1:p.Arg2877=
XM_017010947.2:c.8562A>G	XP_016866436.1:p.Arg2854=
XM_017010948.2:c.8115A>G	XP_016866437.1:p.Arg2705=
XM_017010949.2:c.6966A>G	XP_016866438.1:p.Arg2322=
XM_017010950.1:c.8826A>G	XP_016866439.1:p.Arg2942=
XM_017010951.1:c.*1430A>G	XP_016866440.1:n.*1430A>G
XR_001743469.1:n.9102A>G
NM_138694.4:c.8826A>G MANE Select	NP_619639.3:p.Arg2942=
NM_170724.3:c.8826A>G	NP_733842.2:p.Arg2942=