Canonical Allele Identifier: CA3851102

Gene: PKHD1

Linked Data

• dbSNP Id: rs777144171
• ExAC: 6:51524603 A / G
• gnomAD v2: 6-51524603-A-G
• gnomAD v4: 6-51659805-A-G
• MyVariant Identifiers: chr6:g.51524603A>G (hg19) ; chr6:g.51659805A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659805A>G , CM000668.2:g.51659805A>G	GRCh38
NC_000006.11:g.51524603A>G , CM000668.1:g.51524603A>G	GRCh37
NC_000006.10:g.51632562A>G	NCBI36
NG_008753.1:g.432821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10321T>C MANE Select	ENSP00000360158.3:p.Phe3441Leu
ENST00000371117.7:c.10321T>C	ENSP00000360158.3:p.Phe3441Leu
NM_138694.3:c.10321T>C	NP_619639.3:p.Phe3441Leu
XM_011514679.1:c.10321T>C	XP_011512981.1:p.Phe3441Leu
XM_011514680.1:c.10321T>C	XP_011512982.1:p.Phe3441Leu
XM_011514681.1:c.10192T>C	XP_011512983.1:p.Phe3398Leu
XM_011514682.1:c.10183T>C	XP_011512984.1:p.Phe3395Leu
XM_011514683.1:c.9679T>C	XP_011512985.1:p.Phe3227Leu
XM_011514684.1:c.9610T>C	XP_011512986.1:p.Phe3204Leu
XM_011514687.1:c.10157-10585T>C	XP_011512989.1:n.10157-10585T>C
XM_011514690.1:c.4396T>C	XP_011512992.1:p.Phe1466Leu
XM_011514691.1:c.4396T>C	XP_011512993.1:p.Phe1466Leu
XR_926870.1:n.535+7432A>G
XR_926871.1:n.403+7432A>G
XR_926872.1:n.535+7432A>G
XM_011514680.3:c.10321T>C	XP_011512982.1:p.Phe3441Leu
XM_011514682.3:c.10183T>C	XP_011512984.1:p.Phe3395Leu
XM_011514683.3:c.9679T>C	XP_011512985.1:p.Phe3227Leu
XM_011514684.3:c.9610T>C	XP_011512986.1:p.Phe3204Leu
XM_011514690.3:c.4396T>C	XP_011512992.1:p.Phe1466Leu
XM_011514691.3:c.4396T>C	XP_011512993.1:p.Phe1466Leu
XM_017010944.2:c.10321T>C	XP_016866433.1:p.Phe3441Leu
XM_017010945.2:c.10246T>C	XP_016866434.1:p.Phe3416Leu
XM_017010946.2:c.10126T>C	XP_016866435.1:p.Phe3376Leu
XM_017010947.2:c.10057T>C	XP_016866436.1:p.Phe3353Leu
XM_017010948.2:c.9610T>C	XP_016866437.1:p.Phe3204Leu
XM_017010949.2:c.8461T>C	XP_016866438.1:p.Phe2821Leu
XR_001743469.1:n.10597T>C
XR_001744157.1:n.3145+7432A>G
XR_926870.2:n.3145+7432A>G
XR_926871.2:n.3013+7432A>G
XR_926872.2:n.3145+7432A>G
NM_138694.4:c.10321T>C MANE Select	NP_619639.3:p.Phe3441Leu