Canonical Allele Identifier: CA364420973

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51612936G>C (hg19) ; chr6:g.51748138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748138G>C , CM000668.2:g.51748138G>C	GRCh38
NC_000006.11:g.51612936G>C , CM000668.1:g.51612936G>C	GRCh37
NC_000006.10:g.51720895G>C	NCBI36
NG_008753.1:g.344488C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9478C>G MANE Select	ENSP00000360158.3:p.His3160Asp
ENST00000340994.4:c.9478C>G	ENSP00000341097.4:p.His3160Asp
ENST00000371117.7:c.9478C>G	ENSP00000360158.3:p.His3160Asp
NM_138694.3:c.9478C>G	NP_619639.3:p.His3160Asp
NM_170724.2:c.9478C>G	NP_733842.2:p.His3160Asp
XM_011514679.1:c.9478C>G	XP_011512981.1:p.His3160Asp
XM_011514680.1:c.9478C>G	XP_011512982.1:p.His3160Asp
XM_011514681.1:c.9349C>G	XP_011512983.1:p.His3117Asp
XM_011514682.1:c.9340C>G	XP_011512984.1:p.His3114Asp
XM_011514683.1:c.8836C>G	XP_011512985.1:p.His2946Asp
XM_011514684.1:c.8767C>G	XP_011512986.1:p.His2923Asp
XM_011514685.1:c.9478C>G	XP_011512987.1:p.His3160Asp
XM_011514686.1:c.9478C>G	XP_011512988.1:p.His3160Asp
XM_011514687.1:c.9478C>G	XP_011512989.1:p.His3160Asp
XM_011514688.1:c.9478C>G	XP_011512990.1:p.His3160Asp
XM_011514690.1:c.3553C>G	XP_011512992.1:p.His1185Asp
XM_011514691.1:c.3553C>G	XP_011512993.1:p.His1185Asp
XM_011514680.3:c.9478C>G	XP_011512982.1:p.His3160Asp
XM_011514682.3:c.9340C>G	XP_011512984.1:p.His3114Asp
XM_011514683.3:c.8836C>G	XP_011512985.1:p.His2946Asp
XM_011514684.3:c.8767C>G	XP_011512986.1:p.His2923Asp
XM_011514686.2:c.9478C>G	XP_011512988.1:p.His3160Asp
XM_011514688.2:c.9478C>G	XP_011512990.1:p.His3160Asp
XM_011514690.3:c.3553C>G	XP_011512992.1:p.His1185Asp
XM_011514691.3:c.3553C>G	XP_011512993.1:p.His1185Asp
XM_017010944.2:c.9478C>G	XP_016866433.1:p.His3160Asp
XM_017010945.2:c.9403C>G	XP_016866434.1:p.His3135Asp
XM_017010946.2:c.9283C>G	XP_016866435.1:p.His3095Asp
XM_017010947.2:c.9214C>G	XP_016866436.1:p.His3072Asp
XM_017010948.2:c.8767C>G	XP_016866437.1:p.His2923Asp
XM_017010949.2:c.7618C>G	XP_016866438.1:p.His2540Asp
XM_017010950.1:c.9478C>G	XP_016866439.1:p.His3160Asp
XR_001743469.1:n.9754C>G
NM_138694.4:c.9478C>G MANE Select	NP_619639.3:p.His3160Asp
NM_170724.3:c.9478C>G	NP_733842.2:p.His3160Asp