Canonical Allele Identifier: CA364436344
Gene: PKHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3029648
ClinVar RCV Id: RCV003898908

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659802T>C , CM000668.2:g.51659802T>C GRCh38
NC_000006.11:g.51524600T>C , CM000668.1:g.51524600T>C GRCh37
NC_000006.10:g.51632559T>C NCBI36
NG_008753.1:g.432824A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.10324A>G MANE Select ENSP00000360158.3:p.Ser3442Gly
ENST00000371117.7:c.10324A>G ENSP00000360158.3:p.Ser3442Gly
NM_138694.3:c.10324A>G NP_619639.3:p.Ser3442Gly
XM_011514679.1:c.10324A>G XP_011512981.1:p.Ser3442Gly
XM_011514680.1:c.10324A>G XP_011512982.1:p.Ser3442Gly
XM_011514681.1:c.10195A>G XP_011512983.1:p.Ser3399Gly
XM_011514682.1:c.10186A>G XP_011512984.1:p.Ser3396Gly
XM_011514683.1:c.9682A>G XP_011512985.1:p.Ser3228Gly
XM_011514684.1:c.9613A>G XP_011512986.1:p.Ser3205Gly
XM_011514687.1:c.10157-10582A>G XP_011512989.1:n.10157-10582A>G
XM_011514690.1:c.4399A>G XP_011512992.1:p.Ser1467Gly
XM_011514691.1:c.4399A>G XP_011512993.1:p.Ser1467Gly
XR_926870.1:n.535+7429T>C
XR_926871.1:n.403+7429T>C
XR_926872.1:n.535+7429T>C
XM_011514680.3:c.10324A>G XP_011512982.1:p.Ser3442Gly
XM_011514682.3:c.10186A>G XP_011512984.1:p.Ser3396Gly
XM_011514683.3:c.9682A>G XP_011512985.1:p.Ser3228Gly
XM_011514684.3:c.9613A>G XP_011512986.1:p.Ser3205Gly
XM_011514690.3:c.4399A>G XP_011512992.1:p.Ser1467Gly
XM_011514691.3:c.4399A>G XP_011512993.1:p.Ser1467Gly
XM_017010944.2:c.10324A>G XP_016866433.1:p.Ser3442Gly
XM_017010945.2:c.10249A>G XP_016866434.1:p.Ser3417Gly
XM_017010946.2:c.10129A>G XP_016866435.1:p.Ser3377Gly
XM_017010947.2:c.10060A>G XP_016866436.1:p.Ser3354Gly
XM_017010948.2:c.9613A>G XP_016866437.1:p.Ser3205Gly
XM_017010949.2:c.8464A>G XP_016866438.1:p.Ser2822Gly
XR_001743469.1:n.10600A>G
XR_001744157.1:n.3145+7429T>C
XR_926870.2:n.3145+7429T>C
XR_926871.2:n.3013+7429T>C
XR_926872.2:n.3145+7429T>C
NM_138694.4:c.10324A>G MANE Select NP_619639.3:p.Ser3442Gly