Canonical Allele Identifier: CA2549254085

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51626839T>A , CM000668.2:g.51626839T>A	GRCh38
NC_000006.11:g.51491637T>A , CM000668.1:g.51491637T>A	GRCh37
NC_000006.10:g.51599596T>A	NCBI36
NG_008753.1:g.465787A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.11785+158A>T MANE Select	ENSP00000360158.3:n.11785+158A>T
ENST00000371117.7:c.11785+158A>T	ENSP00000360158.3:n.11785+158A>T
NM_138694.3:c.11785+158A>T	NP_619639.3:n.11785+158A>T
XM_011514679.1:c.11785+158A>T	XP_011512981.1:n.11785+158A>T
XM_011514680.1:c.11785+158A>T	XP_011512982.1:n.11785+158A>T
XM_011514681.1:c.11656+158A>T	XP_011512983.1:n.11656+158A>T
XM_011514682.1:c.11647+158A>T	XP_011512984.1:n.11647+158A>T
XM_011514683.1:c.11143+158A>T	XP_011512985.1:n.11143+158A>T
XM_011514684.1:c.11074+158A>T	XP_011512986.1:n.11074+158A>T
XM_011514690.1:c.5860+158A>T	XP_011512992.1:n.5860+158A>T
XM_011514691.1:c.5860+158A>T	XP_011512993.1:n.5860+158A>T
XM_011514680.3:c.11785+158A>T	XP_011512982.1:n.11785+158A>T
XM_011514682.3:c.11647+158A>T	XP_011512984.1:n.11647+158A>T
XM_011514683.3:c.11143+158A>T	XP_011512985.1:n.11143+158A>T
XM_011514684.3:c.11074+158A>T	XP_011512986.1:n.11074+158A>T
XM_011514690.3:c.5860+158A>T	XP_011512992.1:n.5860+158A>T
XM_011514691.3:c.5860+158A>T	XP_011512993.1:n.5860+158A>T
XM_017010944.2:c.11785+158A>T	XP_016866433.1:n.11785+158A>T
XM_017010945.2:c.11710+158A>T	XP_016866434.1:n.11710+158A>T
XM_017010946.2:c.11590+158A>T	XP_016866435.1:n.11590+158A>T
XM_017010947.2:c.11521+158A>T	XP_016866436.1:n.11521+158A>T
XM_017010948.2:c.11074+158A>T	XP_016866437.1:n.11074+158A>T
XM_017010949.2:c.9925+158A>T	XP_016866438.1:n.9925+158A>T
NM_138694.4:c.11785+158A>T MANE Select	NP_619639.3:n.11785+158A>T