Canonical Allele Identifier: CA364431723
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52069461G>C , CM000668.2:g.52069461G>C GRCh38
NC_000006.11:g.51934259G>C , CM000668.1:g.51934259G>C GRCh37
NC_000006.10:g.52042218G>C NCBI36
NG_008753.1:g.23165C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.774C>G MANE Select ENSP00000360158.3:p.His258Gln
ENST00000340994.4:c.774C>G ENSP00000341097.4:p.His258Gln
ENST00000371117.7:c.774C>G ENSP00000360158.3:p.His258Gln
NM_138694.3:c.774C>G NP_619639.3:p.His258Gln
NM_170724.2:c.774C>G NP_733842.2:p.His258Gln
XM_011514679.1:c.774C>G XP_011512981.1:p.His258Gln
XM_011514680.1:c.774C>G XP_011512982.1:p.His258Gln
XM_011514681.1:c.774C>G XP_011512983.1:p.His258Gln
XM_011514682.1:c.774C>G XP_011512984.1:p.His258Gln
XM_011514683.1:c.774C>G XP_011512985.1:p.His258Gln
XM_011514684.1:c.63C>G XP_011512986.1:p.His21Gln
XM_011514685.1:c.774C>G XP_011512987.1:p.His258Gln
XM_011514686.1:c.774C>G XP_011512988.1:p.His258Gln
XM_011514687.1:c.774C>G XP_011512989.1:p.His258Gln
XM_011514688.1:c.774C>G XP_011512990.1:p.His258Gln
XM_011514689.1:c.774C>G XP_011512991.1:p.His258Gln
XR_926869.1:n.389+265G>C
XM_011514680.3:c.774C>G XP_011512982.1:p.His258Gln
XM_011514682.3:c.774C>G XP_011512984.1:p.His258Gln
XM_011514683.3:c.774C>G XP_011512985.1:p.His258Gln
XM_011514684.3:c.63C>G XP_011512986.1:p.His21Gln
XM_011514686.2:c.774C>G XP_011512988.1:p.His258Gln
XM_011514688.2:c.774C>G XP_011512990.1:p.His258Gln
XM_017010944.2:c.774C>G XP_016866433.1:p.His258Gln
XM_017010945.2:c.699C>G XP_016866434.1:p.His233Gln
XM_017010946.2:c.774C>G XP_016866435.1:p.His258Gln
XM_017010947.2:c.774C>G XP_016866436.1:p.His258Gln
XM_017010948.2:c.63C>G XP_016866437.1:p.His21Gln
XM_017010950.1:c.774C>G XP_016866439.1:p.His258Gln
XM_017010951.1:c.774C>G XP_016866440.1:p.His258Gln
XM_017010952.1:c.774C>G XP_016866441.1:p.His258Gln
XR_001743469.1:n.1050C>G
NM_138694.4:c.774C>G MANE Select NP_619639.3:p.His258Gln
NM_170724.3:c.774C>G NP_733842.2:p.His258Gln