Canonical Allele Identifier: CA364426932

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51753280T>C , CM000668.2:g.51753280T>C	GRCh38
NC_000006.11:g.51618078T>C , CM000668.1:g.51618078T>C	GRCh37
NC_000006.10:g.51726037T>C	NCBI36
NG_008753.1:g.339346A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_138694.4:c.8871A>G MANE Select	NP_619639.3:p.Ile2957Met
ENST00000371117.8:c.8871A>G MANE Select	ENSP00000360158.3:p.Ile2957Met
NM_138694.3:c.8871A>G	NP_619639.3:p.Ile2957Met
NM_170724.2:c.8871A>G	NP_733842.2:p.Ile2957Met
NM_170724.3:c.8871A>G	NP_733842.2:p.Ile2957Met
ENST00000340994.4:c.8871A>G	ENSP00000341097.4:p.Ile2957Met
ENST00000371117.7:c.8871A>G	ENSP00000360158.3:p.Ile2957Met
XM_011514679.1:c.8871A>G	XP_011512981.1:p.Ile2957Met
XM_011514680.1:c.8871A>G	XP_011512982.1:p.Ile2957Met
XM_011514680.3:c.8871A>G	XP_011512982.1:p.Ile2957Met
XM_011514681.1:c.8742A>G	XP_011512983.1:p.Ile2914Met
XM_011514682.1:c.8733A>G	XP_011512984.1:p.Ile2911Met
XM_011514682.3:c.8733A>G	XP_011512984.1:p.Ile2911Met
XM_011514683.1:c.8229A>G	XP_011512985.1:p.Ile2743Met
XM_011514683.3:c.8229A>G	XP_011512985.1:p.Ile2743Met
XM_011514684.1:c.8160A>G	XP_011512986.1:p.Ile2720Met
XM_011514684.3:c.8160A>G	XP_011512986.1:p.Ile2720Met
XM_011514685.1:c.8871A>G	XP_011512987.1:p.Ile2957Met
XM_011514686.1:c.8871A>G	XP_011512988.1:p.Ile2957Met
XM_011514686.2:c.8871A>G	XP_011512988.1:p.Ile2957Met
XM_011514687.1:c.8871A>G	XP_011512989.1:p.Ile2957Met
XM_011514688.1:c.8871A>G	XP_011512990.1:p.Ile2957Met
XM_011514688.2:c.8871A>G	XP_011512990.1:p.Ile2957Met
XM_011514690.1:c.2946A>G	XP_011512992.1:p.Ile982Met
XM_011514690.3:c.2946A>G	XP_011512992.1:p.Ile982Met
XM_011514691.1:c.2946A>G	XP_011512993.1:p.Ile982Met
XM_011514691.3:c.2946A>G	XP_011512993.1:p.Ile982Met
XM_017010944.2:c.8871A>G	XP_016866433.1:p.Ile2957Met
XM_017010945.2:c.8796A>G	XP_016866434.1:p.Ile2932Met
XM_017010946.2:c.8676A>G	XP_016866435.1:p.Ile2892Met
XM_017010947.2:c.8607A>G	XP_016866436.1:p.Ile2869Met
XM_017010948.2:c.8160A>G	XP_016866437.1:p.Ile2720Met
XM_017010949.2:c.7011A>G	XP_016866438.1:p.Ile2337Met
XM_017010950.1:c.8871A>G	XP_016866439.1:p.Ile2957Met
XM_017010951.1:c.*1475A>G	XP_016866440.1:n.*1475A>G
XR_001743469.1:n.9147A>G