Canonical Allele Identifier: CA364418451
Gene: PKHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.51627022T>G , CM000668.2:g.51627022T>G GRCh38
NC_000006.11:g.51491820T>G , CM000668.1:g.51491820T>G GRCh37
NC_000006.10:g.51599779T>G NCBI36
NG_008753.1:g.465604A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371117.8:c.11760A>C MANE Select ENSP00000360158.3:p.Lys3920Asn
ENST00000371117.7:c.11760A>C ENSP00000360158.3:p.Lys3920Asn
NM_138694.3:c.11760A>C NP_619639.3:p.Lys3920Asn
XM_011514679.1:c.11760A>C XP_011512981.1:p.Lys3920Asn
XM_011514680.1:c.11760A>C XP_011512982.1:p.Lys3920Asn
XM_011514681.1:c.11631A>C XP_011512983.1:p.Lys3877Asn
XM_011514682.1:c.11622A>C XP_011512984.1:p.Lys3874Asn
XM_011514683.1:c.11118A>C XP_011512985.1:p.Lys3706Asn
XM_011514684.1:c.11049A>C XP_011512986.1:p.Lys3683Asn
XM_011514690.1:c.5835A>C XP_011512992.1:p.Lys1945Asn
XM_011514691.1:c.5835A>C XP_011512993.1:p.Lys1945Asn
XM_011514680.3:c.11760A>C XP_011512982.1:p.Lys3920Asn
XM_011514682.3:c.11622A>C XP_011512984.1:p.Lys3874Asn
XM_011514683.3:c.11118A>C XP_011512985.1:p.Lys3706Asn
XM_011514684.3:c.11049A>C XP_011512986.1:p.Lys3683Asn
XM_011514690.3:c.5835A>C XP_011512992.1:p.Lys1945Asn
XM_011514691.3:c.5835A>C XP_011512993.1:p.Lys1945Asn
XM_017010944.2:c.11760A>C XP_016866433.1:p.Lys3920Asn
XM_017010945.2:c.11685A>C XP_016866434.1:p.Lys3895Asn
XM_017010946.2:c.11565A>C XP_016866435.1:p.Lys3855Asn
XM_017010947.2:c.11496A>C XP_016866436.1:p.Lys3832Asn
XM_017010948.2:c.11049A>C XP_016866437.1:p.Lys3683Asn
XM_017010949.2:c.9900A>C XP_016866438.1:p.Lys3300Asn
NM_138694.4:c.11760A>C MANE Select NP_619639.3:p.Lys3920Asn