Canonical Allele Identifier: CA3851983
Community Standard Title: NM_138694.4(PKHD1):c.7284C>T (p.Asp2428=)
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51883159G>A , CM000668.2:g.51883159G>A GRCh38
NC_000006.11:g.51747957G>A , CM000668.1:g.51747957G>A GRCh37
NC_000006.10:g.51855916G>A NCBI36
NG_008753.1:g.209467C>T

Transcript Alleles

HGVS Amino-acid Change
NM_138694.4:c.7284C>T MANE Select NP_619639.3:p.Asp2428=
ENST00000371117.8:c.7284C>T MANE Select ENSP00000360158.3:p.Asp2428=
NM_138694.3:c.7284C>T NP_619639.3:p.Asp2428=
NM_170724.2:c.7284C>T NP_733842.2:p.Asp2428=
NM_170724.3:c.7284C>T NP_733842.2:p.Asp2428=
ENST00000340994.4:c.7284C>T ENSP00000341097.4:p.Asp2428=
ENST00000371117.7:c.7284C>T ENSP00000360158.3:p.Asp2428=
XM_011514679.1:c.7284C>T XP_011512981.1:p.Asp2428=
XM_011514680.1:c.7284C>T XP_011512982.1:p.Asp2428=
XM_011514680.3:c.7284C>T XP_011512982.1:p.Asp2428=
XM_011514681.1:c.7284C>T XP_011512983.1:p.Asp2428=
XM_011514682.1:c.7284C>T XP_011512984.1:p.Asp2428=
XM_011514682.3:c.7284C>T XP_011512984.1:p.Asp2428=
XM_011514683.1:c.6642C>T XP_011512985.1:p.Asp2214=
XM_011514683.3:c.6642C>T XP_011512985.1:p.Asp2214=
XM_011514684.1:c.6573C>T XP_011512986.1:p.Asp2191=
XM_011514684.3:c.6573C>T XP_011512986.1:p.Asp2191=
XM_011514685.1:c.7284C>T XP_011512987.1:p.Asp2428=
XM_011514686.1:c.7284C>T XP_011512988.1:p.Asp2428=
XM_011514686.2:c.7284C>T XP_011512988.1:p.Asp2428=
XM_011514687.1:c.7284C>T XP_011512989.1:p.Asp2428=
XM_011514688.1:c.7284C>T XP_011512990.1:p.Asp2428=
XM_011514688.2:c.7284C>T XP_011512990.1:p.Asp2428=
XM_011514689.1:c.7284C>T XP_011512991.1:p.Asp2428=
XM_011514690.1:c.1359C>T XP_011512992.1:p.Asp453=
XM_011514690.3:c.1359C>T XP_011512992.1:p.Asp453=
XM_011514691.1:c.1359C>T XP_011512993.1:p.Asp453=
XM_011514691.3:c.1359C>T XP_011512993.1:p.Asp453=
XM_017010944.2:c.7284C>T XP_016866433.1:p.Asp2428=
XM_017010945.2:c.7209C>T XP_016866434.1:p.Asp2403=
XM_017010946.2:c.7284C>T XP_016866435.1:p.Asp2428=
XM_017010947.2:c.7020C>T XP_016866436.1:p.Asp2340=
XM_017010948.2:c.6573C>T XP_016866437.1:p.Asp2191=
XM_017010949.2:c.5424C>T XP_016866438.1:p.Asp1808=
XM_017010950.1:c.7284C>T XP_016866439.1:p.Asp2428=
XM_017010951.1:c.7284C>T XP_016866440.1:p.Asp2428=
XM_017010952.1:c.7284C>T XP_016866441.1:p.Asp2428=
XR_001743469.1:n.7560C>T