Canonical Allele Identifier: CA2771046790

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51626761_51626904del , CM000668.2:g.51626761_51626904del	GRCh38
NC_000006.11:g.51491559_51491702del , CM000668.1:g.51491559_51491702del	GRCh37
NC_000006.10:g.51599518_51599661del	NCBI36
NG_008753.1:g.465730_465873del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.11785+101_11785+244del MANE Select	ENSP00000360158.3:n.11785+101_11785+244del
ENST00000371117.7:c.11785+101_11785+244del	ENSP00000360158.3:n.11785+101_11785+244del
NM_138694.3:c.11785+101_11785+244del	NP_619639.3:n.11785+101_11785+244del
XM_011514679.1:c.11785+101_11785+244del	XP_011512981.1:n.11785+101_11785+244del
XM_011514680.1:c.11785+101_11785+244del	XP_011512982.1:n.11785+101_11785+244del
XM_011514681.1:c.11656+101_11656+244del	XP_011512983.1:n.11656+101_11656+244del
XM_011514682.1:c.11647+101_11647+244del	XP_011512984.1:n.11647+101_11647+244del
XM_011514683.1:c.11143+101_11143+244del	XP_011512985.1:n.11143+101_11143+244del
XM_011514684.1:c.11074+101_11074+244del	XP_011512986.1:n.11074+101_11074+244del
XM_011514690.1:c.5860+101_5860+244del	XP_011512992.1:n.5860+101_5860+244del
XM_011514691.1:c.5860+101_5860+244del	XP_011512993.1:n.5860+101_5860+244del
XM_011514680.3:c.11785+101_11785+244del	XP_011512982.1:n.11785+101_11785+244del
XM_011514682.3:c.11647+101_11647+244del	XP_011512984.1:n.11647+101_11647+244del
XM_011514683.3:c.11143+101_11143+244del	XP_011512985.1:n.11143+101_11143+244del
XM_011514684.3:c.11074+101_11074+244del	XP_011512986.1:n.11074+101_11074+244del
XM_011514690.3:c.5860+101_5860+244del	XP_011512992.1:n.5860+101_5860+244del
XM_011514691.3:c.5860+101_5860+244del	XP_011512993.1:n.5860+101_5860+244del
XM_017010944.2:c.11785+101_11785+244del	XP_016866433.1:n.11785+101_11785+244del
XM_017010945.2:c.11710+101_11710+244del	XP_016866434.1:n.11710+101_11710+244del
XM_017010946.2:c.11590+101_11590+244del	XP_016866435.1:n.11590+101_11590+244del
XM_017010947.2:c.11521+101_11521+244del	XP_016866436.1:n.11521+101_11521+244del
XM_017010948.2:c.11074+101_11074+244del	XP_016866437.1:n.11074+101_11074+244del
XM_017010949.2:c.9925+101_9925+244del	XP_016866438.1:n.9925+101_9925+244del
NM_138694.4:c.11785+101_11785+244del MANE Select	NP_619639.3:n.11785+101_11785+244del