Canonical Allele Identifier: CA3851092

Gene: PKHD1

Linked Data

• dbSNP Id: rs760790892
• ExAC: 6:51524552 T / C
• gnomAD v2: 6-51524552-T-C
• gnomAD v3: 6-51659754-T-C
• gnomAD v4: 6-51659754-T-C
• MyVariant Identifiers: chr6:g.51524552T>C (hg19) ; chr6:g.51659754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659754T>C , CM000668.2:g.51659754T>C	GRCh38
NC_000006.11:g.51524552T>C , CM000668.1:g.51524552T>C	GRCh37
NC_000006.10:g.51632511T>C	NCBI36
NG_008753.1:g.432872A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10372A>G MANE Select	ENSP00000360158.3:p.Thr3458Ala
ENST00000371117.7:c.10372A>G	ENSP00000360158.3:p.Thr3458Ala
NM_138694.3:c.10372A>G	NP_619639.3:p.Thr3458Ala
XM_011514679.1:c.10372A>G	XP_011512981.1:p.Thr3458Ala
XM_011514680.1:c.10372A>G	XP_011512982.1:p.Thr3458Ala
XM_011514681.1:c.10243A>G	XP_011512983.1:p.Thr3415Ala
XM_011514682.1:c.10234A>G	XP_011512984.1:p.Thr3412Ala
XM_011514683.1:c.9730A>G	XP_011512985.1:p.Thr3244Ala
XM_011514684.1:c.9661A>G	XP_011512986.1:p.Thr3221Ala
XM_011514687.1:c.10157-10534A>G	XP_011512989.1:n.10157-10534A>G
XM_011514690.1:c.4447A>G	XP_011512992.1:p.Thr1483Ala
XM_011514691.1:c.4447A>G	XP_011512993.1:p.Thr1483Ala
XR_926870.1:n.535+7381T>C
XR_926871.1:n.403+7381T>C
XR_926872.1:n.535+7381T>C
XM_011514680.3:c.10372A>G	XP_011512982.1:p.Thr3458Ala
XM_011514682.3:c.10234A>G	XP_011512984.1:p.Thr3412Ala
XM_011514683.3:c.9730A>G	XP_011512985.1:p.Thr3244Ala
XM_011514684.3:c.9661A>G	XP_011512986.1:p.Thr3221Ala
XM_011514690.3:c.4447A>G	XP_011512992.1:p.Thr1483Ala
XM_011514691.3:c.4447A>G	XP_011512993.1:p.Thr1483Ala
XM_017010944.2:c.10372A>G	XP_016866433.1:p.Thr3458Ala
XM_017010945.2:c.10297A>G	XP_016866434.1:p.Thr3433Ala
XM_017010946.2:c.10177A>G	XP_016866435.1:p.Thr3393Ala
XM_017010947.2:c.10108A>G	XP_016866436.1:p.Thr3370Ala
XM_017010948.2:c.9661A>G	XP_016866437.1:p.Thr3221Ala
XM_017010949.2:c.8512A>G	XP_016866438.1:p.Thr2838Ala
XR_001743469.1:n.10648A>G
XR_001744157.1:n.3145+7381T>C
XR_926870.2:n.3145+7381T>C
XR_926871.2:n.3013+7381T>C
XR_926872.2:n.3145+7381T>C
NM_138694.4:c.10372A>G MANE Select	NP_619639.3:p.Thr3458Ala