Canonical Allele Identifier: CA364432084
Gene: PKHD1 HGNC NCBI

Linked Data

gnomAD v4: 6-52025167-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52025167T>A , CM000668.2:g.52025167T>A GRCh38
NC_000006.11:g.51889965T>A , CM000668.1:g.51889965T>A GRCh37
NC_000006.10:g.51997924T>A NCBI36
NG_008753.1:g.67459A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371117.8:c.4643A>T MANE Select ENSP00000360158.3:p.His1548Leu
ENST00000340994.4:c.4643A>T ENSP00000341097.4:p.His1548Leu
ENST00000371117.7:c.4643A>T ENSP00000360158.3:p.His1548Leu
NM_138694.3:c.4643A>T NP_619639.3:p.His1548Leu
NM_170724.2:c.4643A>T NP_733842.2:p.His1548Leu
XM_011514679.1:c.4643A>T XP_011512981.1:p.His1548Leu
XM_011514680.1:c.4643A>T XP_011512982.1:p.His1548Leu
XM_011514681.1:c.4643A>T XP_011512983.1:p.His1548Leu
XM_011514682.1:c.4643A>T XP_011512984.1:p.His1548Leu
XM_011514683.1:c.4102-101A>T XP_011512985.1:n.4102-101A>T
XM_011514684.1:c.3932A>T XP_011512986.1:p.His1311Leu
XM_011514685.1:c.4643A>T XP_011512987.1:p.His1548Leu
XM_011514686.1:c.4643A>T XP_011512988.1:p.His1548Leu
XM_011514687.1:c.4643A>T XP_011512989.1:p.His1548Leu
XM_011514688.1:c.4643A>T XP_011512990.1:p.His1548Leu
XM_011514689.1:c.4643A>T XP_011512991.1:p.His1548Leu
XM_011514680.3:c.4643A>T XP_011512982.1:p.His1548Leu
XM_011514682.3:c.4643A>T XP_011512984.1:p.His1548Leu
XM_011514683.3:c.4102-101A>T XP_011512985.1:n.4102-101A>T
XM_011514684.3:c.3932A>T XP_011512986.1:p.His1311Leu
XM_011514686.2:c.4643A>T XP_011512988.1:p.His1548Leu
XM_011514688.2:c.4643A>T XP_011512990.1:p.His1548Leu
XM_017010944.2:c.4643A>T XP_016866433.1:p.His1548Leu
XM_017010945.2:c.4568A>T XP_016866434.1:p.His1523Leu
XM_017010946.2:c.4643A>T XP_016866435.1:p.His1548Leu
XM_017010947.2:c.4379A>T XP_016866436.1:p.His1460Leu
XM_017010948.2:c.3932A>T XP_016866437.1:p.His1311Leu
XM_017010949.2:c.2783A>T XP_016866438.1:p.His928Leu
XM_017010950.1:c.4643A>T XP_016866439.1:p.His1548Leu
XM_017010951.1:c.4643A>T XP_016866440.1:p.His1548Leu
XM_017010952.1:c.4643A>T XP_016866441.1:p.His1548Leu
XR_001743469.1:n.4919A>T
NM_138694.4:c.4643A>T MANE Select NP_619639.3:p.His1548Leu
NM_170724.3:c.4643A>T NP_733842.2:p.His1548Leu