Canonical Allele Identifier: CA364418788
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627059T>A , CM000668.2:g.51627059T>A GRCh38
NC_000006.11:g.51491857T>A , CM000668.1:g.51491857T>A GRCh37
NC_000006.10:g.51599816T>A NCBI36
NG_008753.1:g.465567A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11723A>T MANE Select ENSP00000360158.3:p.His3908Leu
ENST00000371117.7:c.11723A>T ENSP00000360158.3:p.His3908Leu
NM_138694.3:c.11723A>T NP_619639.3:p.His3908Leu
XM_011514679.1:c.11723A>T XP_011512981.1:p.His3908Leu
XM_011514680.1:c.11723A>T XP_011512982.1:p.His3908Leu
XM_011514681.1:c.11594A>T XP_011512983.1:p.His3865Leu
XM_011514682.1:c.11585A>T XP_011512984.1:p.His3862Leu
XM_011514683.1:c.11081A>T XP_011512985.1:p.His3694Leu
XM_011514684.1:c.11012A>T XP_011512986.1:p.His3671Leu
XM_011514690.1:c.5798A>T XP_011512992.1:p.His1933Leu
XM_011514691.1:c.5798A>T XP_011512993.1:p.His1933Leu
XM_011514680.3:c.11723A>T XP_011512982.1:p.His3908Leu
XM_011514682.3:c.11585A>T XP_011512984.1:p.His3862Leu
XM_011514683.3:c.11081A>T XP_011512985.1:p.His3694Leu
XM_011514684.3:c.11012A>T XP_011512986.1:p.His3671Leu
XM_011514690.3:c.5798A>T XP_011512992.1:p.His1933Leu
XM_011514691.3:c.5798A>T XP_011512993.1:p.His1933Leu
XM_017010944.2:c.11723A>T XP_016866433.1:p.His3908Leu
XM_017010945.2:c.11648A>T XP_016866434.1:p.His3883Leu
XM_017010946.2:c.11528A>T XP_016866435.1:p.His3843Leu
XM_017010947.2:c.11459A>T XP_016866436.1:p.His3820Leu
XM_017010948.2:c.11012A>T XP_016866437.1:p.His3671Leu
XM_017010949.2:c.9863A>T XP_016866438.1:p.His3288Leu
NM_138694.4:c.11723A>T MANE Select NP_619639.3:p.His3908Leu