Canonical Allele Identifier: CA3851606

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51775844G>A , CM000668.2:g.51775844G>A	GRCh38
NC_000006.11:g.51640642G>A , CM000668.1:g.51640642G>A	GRCh37
NC_000006.10:g.51748601G>A	NCBI36
NG_008753.1:g.316782C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138694.4:c.8518C>T MANE Select	NP_619639.3:p.Arg2840Cys
ENST00000371117.8:c.8518C>T MANE Select	ENSP00000360158.3:p.Arg2840Cys
NM_138694.3:c.8518C>T	NP_619639.3:p.Arg2840Cys
NM_170724.2:c.8518C>T	NP_733842.2:p.Arg2840Cys
NM_170724.3:c.8518C>T	NP_733842.2:p.Arg2840Cys
ENST00000340994.4:c.8518C>T	ENSP00000341097.4:p.Arg2840Cys
ENST00000371117.7:c.8518C>T	ENSP00000360158.3:p.Arg2840Cys
XM_011514679.1:c.8518C>T	XP_011512981.1:p.Arg2840Cys
XM_011514680.1:c.8518C>T	XP_011512982.1:p.Arg2840Cys
XM_011514680.3:c.8518C>T	XP_011512982.1:p.Arg2840Cys
XM_011514681.1:c.8389C>T	XP_011512983.1:p.Arg2797Cys
XM_011514682.1:c.8380C>T	XP_011512984.1:p.Arg2794Cys
XM_011514682.3:c.8380C>T	XP_011512984.1:p.Arg2794Cys
XM_011514683.1:c.7876C>T	XP_011512985.1:p.Arg2626Cys
XM_011514683.3:c.7876C>T	XP_011512985.1:p.Arg2626Cys
XM_011514684.1:c.7807C>T	XP_011512986.1:p.Arg2603Cys
XM_011514684.3:c.7807C>T	XP_011512986.1:p.Arg2603Cys
XM_011514685.1:c.8518C>T	XP_011512987.1:p.Arg2840Cys
XM_011514686.1:c.8518C>T	XP_011512988.1:p.Arg2840Cys
XM_011514686.2:c.8518C>T	XP_011512988.1:p.Arg2840Cys
XM_011514687.1:c.8518C>T	XP_011512989.1:p.Arg2840Cys
XM_011514688.1:c.8518C>T	XP_011512990.1:p.Arg2840Cys
XM_011514688.2:c.8518C>T	XP_011512990.1:p.Arg2840Cys
XM_011514690.1:c.2593C>T	XP_011512992.1:p.Arg865Cys
XM_011514690.3:c.2593C>T	XP_011512992.1:p.Arg865Cys
XM_011514691.1:c.2593C>T	XP_011512993.1:p.Arg865Cys
XM_011514691.3:c.2593C>T	XP_011512993.1:p.Arg865Cys
XM_017010944.2:c.8518C>T	XP_016866433.1:p.Arg2840Cys
XM_017010945.2:c.8443C>T	XP_016866434.1:p.Arg2815Cys
XM_017010946.2:c.8323C>T	XP_016866435.1:p.Arg2775Cys
XM_017010947.2:c.8254C>T	XP_016866436.1:p.Arg2752Cys
XM_017010948.2:c.7807C>T	XP_016866437.1:p.Arg2603Cys
XM_017010949.2:c.6658C>T	XP_016866438.1:p.Arg2220Cys
XM_017010950.1:c.8518C>T	XP_016866439.1:p.Arg2840Cys
XM_017010951.1:c.8518C>T	XP_016866440.1:p.Arg2840Cys
XR_001743469.1:n.8794C>T