Canonical Allele Identifier: CA1628647243
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52025156C= , CM000668.2:g.52025156C= GRCh38
NC_000006.11:g.51889954C= , CM000668.1:g.51889954C= GRCh37
NC_000006.10:g.51997913C= NCBI36
NG_008753.1:g.67470G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.4654G= MANE Select ENSP00000360158.3:p.Val1552=
ENST00000340994.4:c.4654G= ENSP00000341097.4:p.Val1552=
ENST00000371117.7:c.4654G= ENSP00000360158.3:p.Val1552=
NM_138694.3:c.4654G= NP_619639.3:p.Val1552=
NM_170724.2:c.4654G= NP_733842.2:p.Val1552=
XM_011514679.1:c.4654G= XP_011512981.1:p.Val1552=
XM_011514680.1:c.4654G= XP_011512982.1:p.Val1552=
XM_011514681.1:c.4654G= XP_011512983.1:p.Val1552=
XM_011514682.1:c.4654G= XP_011512984.1:p.Val1552=
XM_011514683.1:c.4102-90G= XP_011512985.1:n.4102-90G=
XM_011514684.1:c.3943G= XP_011512986.1:p.Val1315=
XM_011514685.1:c.4654G= XP_011512987.1:p.Val1552=
XM_011514686.1:c.4654G= XP_011512988.1:p.Val1552=
XM_011514687.1:c.4654G= XP_011512989.1:p.Val1552=
XM_011514688.1:c.4654G= XP_011512990.1:p.Val1552=
XM_011514689.1:c.4654G= XP_011512991.1:p.Val1552=
XM_011514680.3:c.4654G= XP_011512982.1:p.Val1552=
XM_011514682.3:c.4654G= XP_011512984.1:p.Val1552=
XM_011514683.3:c.4102-90G= XP_011512985.1:n.4102-90G=
XM_011514684.3:c.3943G= XP_011512986.1:p.Val1315=
XM_011514686.2:c.4654G= XP_011512988.1:p.Val1552=
XM_011514688.2:c.4654G= XP_011512990.1:p.Val1552=
XM_017010944.2:c.4654G= XP_016866433.1:p.Val1552=
XM_017010945.2:c.4579G= XP_016866434.1:p.Val1527=
XM_017010946.2:c.4654G= XP_016866435.1:p.Val1552=
XM_017010947.2:c.4390G= XP_016866436.1:p.Val1464=
XM_017010948.2:c.3943G= XP_016866437.1:p.Val1315=
XM_017010949.2:c.2794G= XP_016866438.1:p.Val932=
XM_017010950.1:c.4654G= XP_016866439.1:p.Val1552=
XM_017010951.1:c.4654G= XP_016866440.1:p.Val1552=
XM_017010952.1:c.4654G= XP_016866441.1:p.Val1552=
XR_001743469.1:n.4930G=
NM_138694.4:c.4654G= MANE Select NP_619639.3:p.Val1552=
NM_170724.3:c.4654G= NP_733842.2:p.Val1552=