Canonical Allele Identifier: CA3850737
Gene: PKHD1 HGNC NCBI

Linked Data

dbSNP Id: rs763047969
gnomAD v2: 6-51491900-C-T
gnomAD v4: 6-51627102-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627102C>T , CM000668.2:g.51627102C>T GRCh38
NC_000006.11:g.51491900C>T , CM000668.1:g.51491900C>T GRCh37
NC_000006.10:g.51599859C>T NCBI36
NG_008753.1:g.465524G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11680G>A MANE Select ENSP00000360158.3:p.Glu3894Lys
ENST00000371117.7:c.11680G>A ENSP00000360158.3:p.Glu3894Lys
NM_138694.3:c.11680G>A NP_619639.3:p.Glu3894Lys
XM_011514679.1:c.11680G>A XP_011512981.1:p.Glu3894Lys
XM_011514680.1:c.11680G>A XP_011512982.1:p.Glu3894Lys
XM_011514681.1:c.11551G>A XP_011512983.1:p.Glu3851Lys
XM_011514682.1:c.11542G>A XP_011512984.1:p.Glu3848Lys
XM_011514683.1:c.11038G>A XP_011512985.1:p.Glu3680Lys
XM_011514684.1:c.10969G>A XP_011512986.1:p.Glu3657Lys
XM_011514690.1:c.5755G>A XP_011512992.1:p.Glu1919Lys
XM_011514691.1:c.5755G>A XP_011512993.1:p.Glu1919Lys
XM_011514680.3:c.11680G>A XP_011512982.1:p.Glu3894Lys
XM_011514682.3:c.11542G>A XP_011512984.1:p.Glu3848Lys
XM_011514683.3:c.11038G>A XP_011512985.1:p.Glu3680Lys
XM_011514684.3:c.10969G>A XP_011512986.1:p.Glu3657Lys
XM_011514690.3:c.5755G>A XP_011512992.1:p.Glu1919Lys
XM_011514691.3:c.5755G>A XP_011512993.1:p.Glu1919Lys
XM_017010944.2:c.11680G>A XP_016866433.1:p.Glu3894Lys
XM_017010945.2:c.11605G>A XP_016866434.1:p.Glu3869Lys
XM_017010946.2:c.11485G>A XP_016866435.1:p.Glu3829Lys
XM_017010947.2:c.11416G>A XP_016866436.1:p.Glu3806Lys
XM_017010948.2:c.10969G>A XP_016866437.1:p.Glu3657Lys
XM_017010949.2:c.9820G>A XP_016866438.1:p.Glu3274Lys
NM_138694.4:c.11680G>A MANE Select NP_619639.3:p.Glu3894Lys