Canonical Allele Identifier: CA10624368

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 357379
• ClinVar RCV Id: RCV000316479
• dbSNP Id: rs886061599
• MyVariant Identifiers: chr6:g.51482130G>A (hg19) ; chr6:g.51617332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51617332G>A , CM000668.2:g.51617332G>A	GRCh38
NC_000006.11:g.51482130G>A , CM000668.1:g.51482130G>A	GRCh37
NC_000006.10:g.51590089G>A	NCBI36
NG_008753.1:g.475294C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.*1749C>T MANE Select	ENSP00000360158.3:n.*1749C>T
ENST00000371117.7:c.*1749C>T	ENSP00000360158.3:n.*1749C>T
NM_138694.3:c.*1749C>T	NP_619639.3:n.*1749C>T
XM_011514679.1:c.*1749C>T	XP_011512981.1:n.*1749C>T
XM_011514680.1:c.*1749C>T	XP_011512982.1:n.*1749C>T
XM_011514681.1:c.*1749C>T	XP_011512983.1:n.*1749C>T
XM_011514682.1:c.*1749C>T	XP_011512984.1:n.*1749C>T
XM_011514683.1:c.*1749C>T	XP_011512985.1:n.*1749C>T
XM_011514684.1:c.*1749C>T	XP_011512986.1:n.*1749C>T
XM_011514690.1:c.*1749C>T	XP_011512992.1:n.*1749C>T
XM_011514691.1:c.*1749C>T	XP_011512993.1:n.*1749C>T
XM_011514680.3:c.*1749C>T	XP_011512982.1:n.*1749C>T
XM_011514682.3:c.*1749C>T	XP_011512984.1:n.*1749C>T
XM_011514683.3:c.*1749C>T	XP_011512985.1:n.*1749C>T
XM_011514684.3:c.*1749C>T	XP_011512986.1:n.*1749C>T
XM_011514690.3:c.*1749C>T	XP_011512992.1:n.*1749C>T
XM_011514691.3:c.*1749C>T	XP_011512993.1:n.*1749C>T
XM_017010944.2:c.*1749C>T	XP_016866433.1:n.*1749C>T
XM_017010945.2:c.*1749C>T	XP_016866434.1:n.*1749C>T
XM_017010946.2:c.*1749C>T	XP_016866435.1:n.*1749C>T
XM_017010947.2:c.*1749C>T	XP_016866436.1:n.*1749C>T
XM_017010948.2:c.*1749C>T	XP_016866437.1:n.*1749C>T
XM_017010949.2:c.*1749C>T	XP_016866438.1:n.*1749C>T
NM_138694.4:c.*1749C>T MANE Select	NP_619639.3:n.*1749C>T