Canonical Allele Identifier: CA364426978

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51753288G>A , CM000668.2:g.51753288G>A	GRCh38
NC_000006.11:g.51618086G>A , CM000668.1:g.51618086G>A	GRCh37
NC_000006.10:g.51726045G>A	NCBI36
NG_008753.1:g.339338C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138694.4:c.8863C>T MANE Select	NP_619639.3:p.Arg2955Ter
ENST00000371117.8:c.8863C>T MANE Select	ENSP00000360158.3:p.Arg2955Ter
NM_138694.3:c.8863C>T	NP_619639.3:p.Arg2955Ter
NM_170724.2:c.8863C>T	NP_733842.2:p.Arg2955Ter
NM_170724.3:c.8863C>T	NP_733842.2:p.Arg2955Ter
ENST00000340994.4:c.8863C>T	ENSP00000341097.4:p.Arg2955Ter
ENST00000371117.7:c.8863C>T	ENSP00000360158.3:p.Arg2955Ter
XM_011514679.1:c.8863C>T	XP_011512981.1:p.Arg2955Ter
XM_011514680.1:c.8863C>T	XP_011512982.1:p.Arg2955Ter
XM_011514680.3:c.8863C>T	XP_011512982.1:p.Arg2955Ter
XM_011514681.1:c.8734C>T	XP_011512983.1:p.Arg2912Ter
XM_011514682.1:c.8725C>T	XP_011512984.1:p.Arg2909Ter
XM_011514682.3:c.8725C>T	XP_011512984.1:p.Arg2909Ter
XM_011514683.1:c.8221C>T	XP_011512985.1:p.Arg2741Ter
XM_011514683.3:c.8221C>T	XP_011512985.1:p.Arg2741Ter
XM_011514684.1:c.8152C>T	XP_011512986.1:p.Arg2718Ter
XM_011514684.3:c.8152C>T	XP_011512986.1:p.Arg2718Ter
XM_011514685.1:c.8863C>T	XP_011512987.1:p.Arg2955Ter
XM_011514686.1:c.8863C>T	XP_011512988.1:p.Arg2955Ter
XM_011514686.2:c.8863C>T	XP_011512988.1:p.Arg2955Ter
XM_011514687.1:c.8863C>T	XP_011512989.1:p.Arg2955Ter
XM_011514688.1:c.8863C>T	XP_011512990.1:p.Arg2955Ter
XM_011514688.2:c.8863C>T	XP_011512990.1:p.Arg2955Ter
XM_011514690.1:c.2938C>T	XP_011512992.1:p.Arg980Ter
XM_011514690.3:c.2938C>T	XP_011512992.1:p.Arg980Ter
XM_011514691.1:c.2938C>T	XP_011512993.1:p.Arg980Ter
XM_011514691.3:c.2938C>T	XP_011512993.1:p.Arg980Ter
XM_017010944.2:c.8863C>T	XP_016866433.1:p.Arg2955Ter
XM_017010945.2:c.8788C>T	XP_016866434.1:p.Arg2930Ter
XM_017010946.2:c.8668C>T	XP_016866435.1:p.Arg2890Ter
XM_017010947.2:c.8599C>T	XP_016866436.1:p.Arg2867Ter
XM_017010948.2:c.8152C>T	XP_016866437.1:p.Arg2718Ter
XM_017010949.2:c.7003C>T	XP_016866438.1:p.Arg2335Ter
XM_017010950.1:c.8863C>T	XP_016866439.1:p.Arg2955Ter
XM_017010951.1:c.*1467C>T	XP_016866440.1:n.*1467C>T
XR_001743469.1:n.9139C>T