Canonical Allele Identifier: CA334735

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 188368
• ClinVar RCV Id: RCV000168405
• dbSNP Id: rs786204241
• MyVariant Identifiers: chr6:g.51656172C>T (hg19) ; chr6:g.51791374C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51791374C>T , CM000668.2:g.51791374C>T	GRCh38
NC_000006.11:g.51656172C>T , CM000668.1:g.51656172C>T	GRCh37
NC_000006.10:g.51764131C>T	NCBI36
NG_008753.1:g.301252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.8303-1G>A MANE Select	ENSP00000360158.3:n.8303-1G>A
ENST00000340994.4:c.8303-1G>A	ENSP00000341097.4:n.8303-1G>A
ENST00000371117.7:c.8303-1G>A	ENSP00000360158.3:n.8303-1G>A
NM_138694.3:c.8303-1G>A	NP_619639.3:n.8303-1G>A
NM_170724.2:c.8303-1G>A	NP_733842.2:n.8303-1G>A
XM_011514679.1:c.8303-1G>A	XP_011512981.1:n.8303-1G>A
XM_011514680.1:c.8303-1G>A	XP_011512982.1:n.8303-1G>A
XM_011514681.1:c.8174-1G>A	XP_011512983.1:n.8174-1G>A
XM_011514682.1:c.8303-15453G>A	XP_011512984.1:n.8303-15453G>A
XM_011514683.1:c.7661-1G>A	XP_011512985.1:n.7661-1G>A
XM_011514684.1:c.7592-1G>A	XP_011512986.1:n.7592-1G>A
XM_011514685.1:c.8303-1G>A	XP_011512987.1:n.8303-1G>A
XM_011514686.1:c.8303-1G>A	XP_011512988.1:n.8303-1G>A
XM_011514687.1:c.8303-1G>A	XP_011512989.1:n.8303-1G>A
XM_011514688.1:c.8303-1G>A	XP_011512990.1:n.8303-1G>A
XM_011514689.1:c.*9-1G>A	XP_011512991.1:n.*9-1G>A
XM_011514690.1:c.2378-1G>A	XP_011512992.1:n.2378-1G>A
XM_011514691.1:c.2378-1G>A	XP_011512993.1:n.2378-1G>A
XM_011514680.3:c.8303-1G>A	XP_011512982.1:n.8303-1G>A
XM_011514682.3:c.8303-15453G>A	XP_011512984.1:n.8303-15453G>A
XM_011514683.3:c.7661-1G>A	XP_011512985.1:n.7661-1G>A
XM_011514684.3:c.7592-1G>A	XP_011512986.1:n.7592-1G>A
XM_011514686.2:c.8303-1G>A	XP_011512988.1:n.8303-1G>A
XM_011514688.2:c.8303-1G>A	XP_011512990.1:n.8303-1G>A
XM_011514690.3:c.2378-1G>A	XP_011512992.1:n.2378-1G>A
XM_011514691.3:c.2378-1G>A	XP_011512993.1:n.2378-1G>A
XM_017010944.2:c.8303-1G>A	XP_016866433.1:n.8303-1G>A
XM_017010945.2:c.8228-1G>A	XP_016866434.1:n.8228-1G>A
XM_017010946.2:c.8108-1G>A	XP_016866435.1:n.8108-1G>A
XM_017010947.2:c.8039-1G>A	XP_016866436.1:n.8039-1G>A
XM_017010948.2:c.7592-1G>A	XP_016866437.1:n.7592-1G>A
XM_017010949.2:c.6443-1G>A	XP_016866438.1:n.6443-1G>A
XM_017010950.1:c.8303-1G>A	XP_016866439.1:n.8303-1G>A
XM_017010951.1:c.8303-1G>A	XP_016866440.1:n.8303-1G>A
XR_001743469.1:n.8579-1G>A
NM_138694.4:c.8303-1G>A MANE Select	NP_619639.3:n.8303-1G>A
NM_170724.3:c.8303-1G>A	NP_733842.2:n.8303-1G>A