Canonical Allele Identifier: CA3851062
Community Standard Title: NM_138694.4(PKHD1):c.10514G>A (p.Ser3505Asn)
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51659612C>T , CM000668.2:g.51659612C>T GRCh38
NC_000006.11:g.51524410C>T , CM000668.1:g.51524410C>T GRCh37
NC_000006.10:g.51632369C>T NCBI36
NG_008753.1:g.433014G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138694.4:c.10514G>A MANE Select NP_619639.3:p.Ser3505Asn
ENST00000371117.8:c.10514G>A MANE Select ENSP00000360158.3:p.Ser3505Asn
NM_138694.3:c.10514G>A NP_619639.3:p.Ser3505Asn
ENST00000371117.7:c.10514G>A ENSP00000360158.3:p.Ser3505Asn
XM_011514679.1:c.10514G>A XP_011512981.1:p.Ser3505Asn
XM_011514680.1:c.10514G>A XP_011512982.1:p.Ser3505Asn
XM_011514680.3:c.10514G>A XP_011512982.1:p.Ser3505Asn
XM_011514681.1:c.10385G>A XP_011512983.1:p.Ser3462Asn
XM_011514682.1:c.10376G>A XP_011512984.1:p.Ser3459Asn
XM_011514682.3:c.10376G>A XP_011512984.1:p.Ser3459Asn
XM_011514683.1:c.9872G>A XP_011512985.1:p.Ser3291Asn
XM_011514683.3:c.9872G>A XP_011512985.1:p.Ser3291Asn
XM_011514684.1:c.9803G>A XP_011512986.1:p.Ser3268Asn
XM_011514684.3:c.9803G>A XP_011512986.1:p.Ser3268Asn
XM_011514687.1:c.10157-10392G>A XP_011512989.1:n.10157-10392G>A
XM_011514690.1:c.4589G>A XP_011512992.1:p.Ser1530Asn
XM_011514690.3:c.4589G>A XP_011512992.1:p.Ser1530Asn
XM_011514691.1:c.4589G>A XP_011512993.1:p.Ser1530Asn
XM_011514691.3:c.4589G>A XP_011512993.1:p.Ser1530Asn
XM_017010944.2:c.10514G>A XP_016866433.1:p.Ser3505Asn
XM_017010945.2:c.10439G>A XP_016866434.1:p.Ser3480Asn
XM_017010946.2:c.10319G>A XP_016866435.1:p.Ser3440Asn
XM_017010947.2:c.10250G>A XP_016866436.1:p.Ser3417Asn
XM_017010948.2:c.9803G>A XP_016866437.1:p.Ser3268Asn
XM_017010949.2:c.8654G>A XP_016866438.1:p.Ser2885Asn
XR_001743469.1:n.10790G>A
XR_001744157.1:n.3145+7239C>T
XR_926870.1:n.535+7239C>T
XR_926870.2:n.3145+7239C>T
XR_926871.1:n.403+7239C>T
XR_926871.2:n.3013+7239C>T
XR_926872.1:n.535+7239C>T
XR_926872.2:n.3145+7239C>T