Canonical Allele Identifier: CA364418429
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627020T>A , CM000668.2:g.51627020T>A GRCh38
NC_000006.11:g.51491818T>A , CM000668.1:g.51491818T>A GRCh37
NC_000006.10:g.51599777T>A NCBI36
NG_008753.1:g.465606A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11762A>T MANE Select ENSP00000360158.3:p.Lys3921Ile
ENST00000371117.7:c.11762A>T ENSP00000360158.3:p.Lys3921Ile
NM_138694.3:c.11762A>T NP_619639.3:p.Lys3921Ile
XM_011514679.1:c.11762A>T XP_011512981.1:p.Lys3921Ile
XM_011514680.1:c.11762A>T XP_011512982.1:p.Lys3921Ile
XM_011514681.1:c.11633A>T XP_011512983.1:p.Lys3878Ile
XM_011514682.1:c.11624A>T XP_011512984.1:p.Lys3875Ile
XM_011514683.1:c.11120A>T XP_011512985.1:p.Lys3707Ile
XM_011514684.1:c.11051A>T XP_011512986.1:p.Lys3684Ile
XM_011514690.1:c.5837A>T XP_011512992.1:p.Lys1946Ile
XM_011514691.1:c.5837A>T XP_011512993.1:p.Lys1946Ile
XM_011514680.3:c.11762A>T XP_011512982.1:p.Lys3921Ile
XM_011514682.3:c.11624A>T XP_011512984.1:p.Lys3875Ile
XM_011514683.3:c.11120A>T XP_011512985.1:p.Lys3707Ile
XM_011514684.3:c.11051A>T XP_011512986.1:p.Lys3684Ile
XM_011514690.3:c.5837A>T XP_011512992.1:p.Lys1946Ile
XM_011514691.3:c.5837A>T XP_011512993.1:p.Lys1946Ile
XM_017010944.2:c.11762A>T XP_016866433.1:p.Lys3921Ile
XM_017010945.2:c.11687A>T XP_016866434.1:p.Lys3896Ile
XM_017010946.2:c.11567A>T XP_016866435.1:p.Lys3856Ile
XM_017010947.2:c.11498A>T XP_016866436.1:p.Lys3833Ile
XM_017010948.2:c.11051A>T XP_016866437.1:p.Lys3684Ile
XM_017010949.2:c.9902A>T XP_016866438.1:p.Lys3301Ile
NM_138694.4:c.11762A>T MANE Select NP_619639.3:p.Lys3921Ile