Canonical Allele Identifier: CA364416571
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51791359C>G , CM000668.2:g.51791359C>G GRCh38
NC_000006.11:g.51656157C>G , CM000668.1:g.51656157C>G GRCh37
NC_000006.10:g.51764116C>G NCBI36
NG_008753.1:g.301267G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.8317G>C MANE Select ENSP00000360158.3:p.Val2773Leu
ENST00000340994.4:c.8317G>C ENSP00000341097.4:p.Val2773Leu
ENST00000371117.7:c.8317G>C ENSP00000360158.3:p.Val2773Leu
NM_138694.3:c.8317G>C NP_619639.3:p.Val2773Leu
NM_170724.2:c.8317G>C NP_733842.2:p.Val2773Leu
XM_011514679.1:c.8317G>C XP_011512981.1:p.Val2773Leu
XM_011514680.1:c.8317G>C XP_011512982.1:p.Val2773Leu
XM_011514681.1:c.8188G>C XP_011512983.1:p.Val2730Leu
XM_011514682.1:c.8303-15438G>C XP_011512984.1:n.8303-15438G>C
XM_011514683.1:c.7675G>C XP_011512985.1:p.Val2559Leu
XM_011514684.1:c.7606G>C XP_011512986.1:p.Val2536Leu
XM_011514685.1:c.8317G>C XP_011512987.1:p.Val2773Leu
XM_011514686.1:c.8317G>C XP_011512988.1:p.Val2773Leu
XM_011514687.1:c.8317G>C XP_011512989.1:p.Val2773Leu
XM_011514688.1:c.8317G>C XP_011512990.1:p.Val2773Leu
XM_011514689.1:c.*23G>C XP_011512991.1:n.*23G>C
XM_011514690.1:c.2392G>C XP_011512992.1:p.Val798Leu
XM_011514691.1:c.2392G>C XP_011512993.1:p.Val798Leu
XM_011514680.3:c.8317G>C XP_011512982.1:p.Val2773Leu
XM_011514682.3:c.8303-15438G>C XP_011512984.1:n.8303-15438G>C
XM_011514683.3:c.7675G>C XP_011512985.1:p.Val2559Leu
XM_011514684.3:c.7606G>C XP_011512986.1:p.Val2536Leu
XM_011514686.2:c.8317G>C XP_011512988.1:p.Val2773Leu
XM_011514688.2:c.8317G>C XP_011512990.1:p.Val2773Leu
XM_011514690.3:c.2392G>C XP_011512992.1:p.Val798Leu
XM_011514691.3:c.2392G>C XP_011512993.1:p.Val798Leu
XM_017010944.2:c.8317G>C XP_016866433.1:p.Val2773Leu
XM_017010945.2:c.8242G>C XP_016866434.1:p.Val2748Leu
XM_017010946.2:c.8122G>C XP_016866435.1:p.Val2708Leu
XM_017010947.2:c.8053G>C XP_016866436.1:p.Val2685Leu
XM_017010948.2:c.7606G>C XP_016866437.1:p.Val2536Leu
XM_017010949.2:c.6457G>C XP_016866438.1:p.Val2153Leu
XM_017010950.1:c.8317G>C XP_016866439.1:p.Val2773Leu
XM_017010951.1:c.8317G>C XP_016866440.1:p.Val2773Leu
XR_001743469.1:n.8593G>C
NM_138694.4:c.8317G>C MANE Select NP_619639.3:p.Val2773Leu
NM_170724.3:c.8317G>C NP_733842.2:p.Val2773Leu