Canonical Allele Identifier: CA364420763
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51748035T>G , CM000668.2:g.51748035T>G GRCh38
NC_000006.11:g.51612833T>G , CM000668.1:g.51612833T>G GRCh37
NC_000006.10:g.51720792T>G NCBI36
NG_008753.1:g.344591A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.9581A>C MANE Select ENSP00000360158.3:p.Lys3194Thr
ENST00000340994.4:c.9581A>C ENSP00000341097.4:p.Lys3194Thr
ENST00000371117.7:c.9581A>C ENSP00000360158.3:p.Lys3194Thr
NM_138694.3:c.9581A>C NP_619639.3:p.Lys3194Thr
NM_170724.2:c.9581A>C NP_733842.2:p.Lys3194Thr
XM_011514679.1:c.9581A>C XP_011512981.1:p.Lys3194Thr
XM_011514680.1:c.9581A>C XP_011512982.1:p.Lys3194Thr
XM_011514681.1:c.9452A>C XP_011512983.1:p.Lys3151Thr
XM_011514682.1:c.9443A>C XP_011512984.1:p.Lys3148Thr
XM_011514683.1:c.8939A>C XP_011512985.1:p.Lys2980Thr
XM_011514684.1:c.8870A>C XP_011512986.1:p.Lys2957Thr
XM_011514685.1:c.9581A>C XP_011512987.1:p.Lys3194Thr
XM_011514686.1:c.9581A>C XP_011512988.1:p.Lys3194Thr
XM_011514687.1:c.9581A>C XP_011512989.1:p.Lys3194Thr
XM_011514688.1:c.9581A>C XP_011512990.1:p.Lys3194Thr
XM_011514690.1:c.3656A>C XP_011512992.1:p.Lys1219Thr
XM_011514691.1:c.3656A>C XP_011512993.1:p.Lys1219Thr
XM_011514680.3:c.9581A>C XP_011512982.1:p.Lys3194Thr
XM_011514682.3:c.9443A>C XP_011512984.1:p.Lys3148Thr
XM_011514683.3:c.8939A>C XP_011512985.1:p.Lys2980Thr
XM_011514684.3:c.8870A>C XP_011512986.1:p.Lys2957Thr
XM_011514686.2:c.9581A>C XP_011512988.1:p.Lys3194Thr
XM_011514688.2:c.9581A>C XP_011512990.1:p.Lys3194Thr
XM_011514690.3:c.3656A>C XP_011512992.1:p.Lys1219Thr
XM_011514691.3:c.3656A>C XP_011512993.1:p.Lys1219Thr
XM_017010944.2:c.9581A>C XP_016866433.1:p.Lys3194Thr
XM_017010945.2:c.9506A>C XP_016866434.1:p.Lys3169Thr
XM_017010946.2:c.9386A>C XP_016866435.1:p.Lys3129Thr
XM_017010947.2:c.9317A>C XP_016866436.1:p.Lys3106Thr
XM_017010948.2:c.8870A>C XP_016866437.1:p.Lys2957Thr
XM_017010949.2:c.7721A>C XP_016866438.1:p.Lys2574Thr
XM_017010950.1:c.9581A>C XP_016866439.1:p.Lys3194Thr
XR_001743469.1:n.9857A>C
NM_138694.4:c.9581A>C MANE Select NP_619639.3:p.Lys3194Thr
NM_170724.3:c.9581A>C NP_733842.2:p.Lys3194Thr