Canonical Allele Identifier: CA3851053

Gene: PKHD1

Linked Data

• dbSNP Id: rs773006043
• ExAC: 6:51524375 G / T
• gnomAD v2: 6-51524375-G-T
• gnomAD v4: 6-51659577-G-T
• MyVariant Identifiers: chr6:g.51524375G>T (hg19) ; chr6:g.51659577G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659577G>T , CM000668.2:g.51659577G>T	GRCh38
NC_000006.11:g.51524375G>T , CM000668.1:g.51524375G>T	GRCh37
NC_000006.10:g.51632334G>T	NCBI36
NG_008753.1:g.433049C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10549C>A MANE Select	ENSP00000360158.3:p.Pro3517Thr
ENST00000371117.7:c.10549C>A	ENSP00000360158.3:p.Pro3517Thr
NM_138694.3:c.10549C>A	NP_619639.3:p.Pro3517Thr
XM_011514679.1:c.10549C>A	XP_011512981.1:p.Pro3517Thr
XM_011514680.1:c.10549C>A	XP_011512982.1:p.Pro3517Thr
XM_011514681.1:c.10420C>A	XP_011512983.1:p.Pro3474Thr
XM_011514682.1:c.10411C>A	XP_011512984.1:p.Pro3471Thr
XM_011514683.1:c.9907C>A	XP_011512985.1:p.Pro3303Thr
XM_011514684.1:c.9838C>A	XP_011512986.1:p.Pro3280Thr
XM_011514687.1:c.10157-10357C>A	XP_011512989.1:n.10157-10357C>A
XM_011514690.1:c.4624C>A	XP_011512992.1:p.Pro1542Thr
XM_011514691.1:c.4624C>A	XP_011512993.1:p.Pro1542Thr
XR_926870.1:n.535+7204G>T
XR_926871.1:n.403+7204G>T
XR_926872.1:n.535+7204G>T
XM_011514680.3:c.10549C>A	XP_011512982.1:p.Pro3517Thr
XM_011514682.3:c.10411C>A	XP_011512984.1:p.Pro3471Thr
XM_011514683.3:c.9907C>A	XP_011512985.1:p.Pro3303Thr
XM_011514684.3:c.9838C>A	XP_011512986.1:p.Pro3280Thr
XM_011514690.3:c.4624C>A	XP_011512992.1:p.Pro1542Thr
XM_011514691.3:c.4624C>A	XP_011512993.1:p.Pro1542Thr
XM_017010944.2:c.10549C>A	XP_016866433.1:p.Pro3517Thr
XM_017010945.2:c.10474C>A	XP_016866434.1:p.Pro3492Thr
XM_017010946.2:c.10354C>A	XP_016866435.1:p.Pro3452Thr
XM_017010947.2:c.10285C>A	XP_016866436.1:p.Pro3429Thr
XM_017010948.2:c.9838C>A	XP_016866437.1:p.Pro3280Thr
XM_017010949.2:c.8689C>A	XP_016866438.1:p.Pro2897Thr
XR_001743469.1:n.10825C>A
XR_001744157.1:n.3145+7204G>T
XR_926870.2:n.3145+7204G>T
XR_926871.2:n.3013+7204G>T
XR_926872.2:n.3145+7204G>T
NM_138694.4:c.10549C>A MANE Select	NP_619639.3:p.Pro3517Thr