Canonical Allele Identifier: CA1628603077

Gene: PKHD1

Linked Data

• dbSNP Id: rs1808109012

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52058345_52058350dup , CM000668.2:g.52058345_52058350dup	GRCh38
NC_000006.11:g.51923143_51923148dup , CM000668.1:g.51923143_51923148dup	GRCh37
NC_000006.10:g.52031102_52031107dup	NCBI36
NG_008753.1:g.34278_34283dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.1487_1492dup MANE Select	ENSP00000360158.3:p.Ala497_Gln498insArgAla
ENST00000340994.4:c.1487_1492dup	ENSP00000341097.4:p.Ala497_Gln498insArgAla
ENST00000371117.7:c.1487_1492dup	ENSP00000360158.3:p.Ala497_Gln498insArgAla
NM_138694.3:c.1487_1492dup	NP_619639.3:p.Ala497_Gln498insArgAla
NM_170724.2:c.1487_1492dup	NP_733842.2:p.Ala497_Gln498insArgAla
XM_011514679.1:c.1487_1492dup	XP_011512981.1:p.Ala497_Gln498insArgAla
XM_011514680.1:c.1487_1492dup	XP_011512982.1:p.Ala497_Gln498insArgAla
XM_011514681.1:c.1487_1492dup	XP_011512983.1:p.Ala497_Gln498insArgAla
XM_011514682.1:c.1487_1492dup	XP_011512984.1:p.Ala497_Gln498insArgAla
XM_011514683.1:c.1487_1492dup	XP_011512985.1:p.Ala497_Gln498insArgAla
XM_011514684.1:c.776_781dup	XP_011512986.1:p.Ala260_Gln261insArgAla
XM_011514685.1:c.1487_1492dup	XP_011512987.1:p.Ala497_Gln498insArgAla
XM_011514686.1:c.1487_1492dup	XP_011512988.1:p.Ala497_Gln498insArgAla
XM_011514687.1:c.1487_1492dup	XP_011512989.1:p.Ala497_Gln498insArgAla
XM_011514688.1:c.1487_1492dup	XP_011512990.1:p.Ala497_Gln498insArgAla
XM_011514689.1:c.1487_1492dup	XP_011512991.1:p.Ala497_Gln498insArgAla
XM_011514680.3:c.1487_1492dup	XP_011512982.1:p.Ala497_Gln498insArgAla
XM_011514682.3:c.1487_1492dup	XP_011512984.1:p.Ala497_Gln498insArgAla
XM_011514683.3:c.1487_1492dup	XP_011512985.1:p.Ala497_Gln498insArgAla
XM_011514684.3:c.776_781dup	XP_011512986.1:p.Ala260_Gln261insArgAla
XM_011514686.2:c.1487_1492dup	XP_011512988.1:p.Ala497_Gln498insArgAla
XM_011514688.2:c.1487_1492dup	XP_011512990.1:p.Ala497_Gln498insArgAla
XM_017010944.2:c.1487_1492dup	XP_016866433.1:p.Ala497_Gln498insArgAla
XM_017010945.2:c.1412_1417dup	XP_016866434.1:p.Ala472_Gln473insArgAla
XM_017010946.2:c.1487_1492dup	XP_016866435.1:p.Ala497_Gln498insArgAla
XM_017010947.2:c.1487_1492dup	XP_016866436.1:p.Ala497_Gln498insArgAla
XM_017010948.2:c.776_781dup	XP_016866437.1:p.Ala260_Gln261insArgAla
XM_017010950.1:c.1487_1492dup	XP_016866439.1:p.Ala497_Gln498insArgAla
XM_017010951.1:c.1487_1492dup	XP_016866440.1:p.Ala497_Gln498insArgAla
XM_017010952.1:c.1487_1492dup	XP_016866441.1:p.Ala497_Gln498insArgAla
XR_001743469.1:n.1763_1768dup
NM_138694.4:c.1487_1492dup MANE Select	NP_619639.3:p.Ala497_Gln498insArgAla
NM_170724.3:c.1487_1492dup	NP_733842.2:p.Ala497_Gln498insArgAla