Canonical Allele Identifier: CA364427193
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51753331A>C , CM000668.2:g.51753331A>C GRCh38
NC_000006.11:g.51618129A>C , CM000668.1:g.51618129A>C GRCh37
NC_000006.10:g.51726088A>C NCBI36
NG_008753.1:g.339295T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.8820T>G MANE Select ENSP00000360158.3:p.Asp2940Glu
ENST00000340994.4:c.8820T>G ENSP00000341097.4:p.Asp2940Glu
ENST00000371117.7:c.8820T>G ENSP00000360158.3:p.Asp2940Glu
NM_138694.3:c.8820T>G NP_619639.3:p.Asp2940Glu
NM_170724.2:c.8820T>G NP_733842.2:p.Asp2940Glu
XM_011514679.1:c.8820T>G XP_011512981.1:p.Asp2940Glu
XM_011514680.1:c.8820T>G XP_011512982.1:p.Asp2940Glu
XM_011514681.1:c.8691T>G XP_011512983.1:p.Asp2897Glu
XM_011514682.1:c.8682T>G XP_011512984.1:p.Asp2894Glu
XM_011514683.1:c.8178T>G XP_011512985.1:p.Asp2726Glu
XM_011514684.1:c.8109T>G XP_011512986.1:p.Asp2703Glu
XM_011514685.1:c.8820T>G XP_011512987.1:p.Asp2940Glu
XM_011514686.1:c.8820T>G XP_011512988.1:p.Asp2940Glu
XM_011514687.1:c.8820T>G XP_011512989.1:p.Asp2940Glu
XM_011514688.1:c.8820T>G XP_011512990.1:p.Asp2940Glu
XM_011514690.1:c.2895T>G XP_011512992.1:p.Asp965Glu
XM_011514691.1:c.2895T>G XP_011512993.1:p.Asp965Glu
XM_011514680.3:c.8820T>G XP_011512982.1:p.Asp2940Glu
XM_011514682.3:c.8682T>G XP_011512984.1:p.Asp2894Glu
XM_011514683.3:c.8178T>G XP_011512985.1:p.Asp2726Glu
XM_011514684.3:c.8109T>G XP_011512986.1:p.Asp2703Glu
XM_011514686.2:c.8820T>G XP_011512988.1:p.Asp2940Glu
XM_011514688.2:c.8820T>G XP_011512990.1:p.Asp2940Glu
XM_011514690.3:c.2895T>G XP_011512992.1:p.Asp965Glu
XM_011514691.3:c.2895T>G XP_011512993.1:p.Asp965Glu
XM_017010944.2:c.8820T>G XP_016866433.1:p.Asp2940Glu
XM_017010945.2:c.8745T>G XP_016866434.1:p.Asp2915Glu
XM_017010946.2:c.8625T>G XP_016866435.1:p.Asp2875Glu
XM_017010947.2:c.8556T>G XP_016866436.1:p.Asp2852Glu
XM_017010948.2:c.8109T>G XP_016866437.1:p.Asp2703Glu
XM_017010949.2:c.6960T>G XP_016866438.1:p.Asp2320Glu
XM_017010950.1:c.8820T>G XP_016866439.1:p.Asp2940Glu
XM_017010951.1:c.*1424T>G XP_016866440.1:n.*1424T>G
XR_001743469.1:n.9096T>G
NM_138694.4:c.8820T>G MANE Select NP_619639.3:p.Asp2940Glu
NM_170724.3:c.8820T>G NP_733842.2:p.Asp2940Glu