Canonical Allele Identifier: CA364418439
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627021T>C , CM000668.2:g.51627021T>C GRCh38
NC_000006.11:g.51491819T>C , CM000668.1:g.51491819T>C GRCh37
NC_000006.10:g.51599778T>C NCBI36
NG_008753.1:g.465605A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11761A>G MANE Select ENSP00000360158.3:p.Lys3921Glu
ENST00000371117.7:c.11761A>G ENSP00000360158.3:p.Lys3921Glu
NM_138694.3:c.11761A>G NP_619639.3:p.Lys3921Glu
XM_011514679.1:c.11761A>G XP_011512981.1:p.Lys3921Glu
XM_011514680.1:c.11761A>G XP_011512982.1:p.Lys3921Glu
XM_011514681.1:c.11632A>G XP_011512983.1:p.Lys3878Glu
XM_011514682.1:c.11623A>G XP_011512984.1:p.Lys3875Glu
XM_011514683.1:c.11119A>G XP_011512985.1:p.Lys3707Glu
XM_011514684.1:c.11050A>G XP_011512986.1:p.Lys3684Glu
XM_011514690.1:c.5836A>G XP_011512992.1:p.Lys1946Glu
XM_011514691.1:c.5836A>G XP_011512993.1:p.Lys1946Glu
XM_011514680.3:c.11761A>G XP_011512982.1:p.Lys3921Glu
XM_011514682.3:c.11623A>G XP_011512984.1:p.Lys3875Glu
XM_011514683.3:c.11119A>G XP_011512985.1:p.Lys3707Glu
XM_011514684.3:c.11050A>G XP_011512986.1:p.Lys3684Glu
XM_011514690.3:c.5836A>G XP_011512992.1:p.Lys1946Glu
XM_011514691.3:c.5836A>G XP_011512993.1:p.Lys1946Glu
XM_017010944.2:c.11761A>G XP_016866433.1:p.Lys3921Glu
XM_017010945.2:c.11686A>G XP_016866434.1:p.Lys3896Glu
XM_017010946.2:c.11566A>G XP_016866435.1:p.Lys3856Glu
XM_017010947.2:c.11497A>G XP_016866436.1:p.Lys3833Glu
XM_017010948.2:c.11050A>G XP_016866437.1:p.Lys3684Glu
XM_017010949.2:c.9901A>G XP_016866438.1:p.Lys3301Glu
NM_138694.4:c.11761A>G MANE Select NP_619639.3:p.Lys3921Glu