Canonical Allele Identifier: CA1628595315
Gene: PKHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51887096A= , CM000668.2:g.51887096A= GRCh38
NC_000006.11:g.51751894A= , CM000668.1:g.51751894A= GRCh37
NC_000006.10:g.51859853A= NCBI36
NG_008753.1:g.205530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.7109+37T= MANE Select ENSP00000360158.3:n.7109+37T=
ENST00000340994.4:c.7109+37T= ENSP00000341097.4:n.7109+37T=
ENST00000371117.7:c.7109+37T= ENSP00000360158.3:n.7109+37T=
NM_138694.3:c.7109+37T= NP_619639.3:n.7109+37T=
NM_170724.2:c.7109+37T= NP_733842.2:n.7109+37T=
XM_011514679.1:c.7109+37T= XP_011512981.1:n.7109+37T=
XM_011514680.1:c.7109+37T= XP_011512982.1:n.7109+37T=
XM_011514681.1:c.7109+37T= XP_011512983.1:n.7109+37T=
XM_011514682.1:c.7109+37T= XP_011512984.1:n.7109+37T=
XM_011514683.1:c.6467+37T= XP_011512985.1:n.6467+37T=
XM_011514684.1:c.6398+37T= XP_011512986.1:n.6398+37T=
XM_011514685.1:c.7109+37T= XP_011512987.1:n.7109+37T=
XM_011514686.1:c.7109+37T= XP_011512988.1:n.7109+37T=
XM_011514687.1:c.7109+37T= XP_011512989.1:n.7109+37T=
XM_011514688.1:c.7109+37T= XP_011512990.1:n.7109+37T=
XM_011514689.1:c.7109+37T= XP_011512991.1:n.7109+37T=
XM_011514690.1:c.1184+37T= XP_011512992.1:n.1184+37T=
XM_011514691.1:c.1184+37T= XP_011512993.1:n.1184+37T=
XM_011514680.3:c.7109+37T= XP_011512982.1:n.7109+37T=
XM_011514682.3:c.7109+37T= XP_011512984.1:n.7109+37T=
XM_011514683.3:c.6467+37T= XP_011512985.1:n.6467+37T=
XM_011514684.3:c.6398+37T= XP_011512986.1:n.6398+37T=
XM_011514686.2:c.7109+37T= XP_011512988.1:n.7109+37T=
XM_011514688.2:c.7109+37T= XP_011512990.1:n.7109+37T=
XM_011514690.3:c.1184+37T= XP_011512992.1:n.1184+37T=
XM_011514691.3:c.1184+37T= XP_011512993.1:n.1184+37T=
XM_017010944.2:c.7109+37T= XP_016866433.1:n.7109+37T=
XM_017010945.2:c.7034+37T= XP_016866434.1:n.7034+37T=
XM_017010946.2:c.7109+37T= XP_016866435.1:n.7109+37T=
XM_017010947.2:c.6845+37T= XP_016866436.1:n.6845+37T=
XM_017010948.2:c.6398+37T= XP_016866437.1:n.6398+37T=
XM_017010949.2:c.5249+37T= XP_016866438.1:n.5249+37T=
XM_017010950.1:c.7109+37T= XP_016866439.1:n.7109+37T=
XM_017010951.1:c.7109+37T= XP_016866440.1:n.7109+37T=
XM_017010952.1:c.7109+37T= XP_016866441.1:n.7109+37T=
XR_001743469.1:n.7385+37T=
NM_138694.4:c.7109+37T= MANE Select NP_619639.3:n.7109+37T=
NM_170724.3:c.7109+37T= NP_733842.2:n.7109+37T=