Canonical Allele Identifier: CA138910820

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 2777283
• ClinVar RCV Id: RCV003611690
• dbSNP Id: rs975457126
• gnomAD v2: 6-51777202-A-T
• gnomAD v4: 6-51912404-A-T
• MyVariant Identifiers: chr6:g.51777202A>T (hg19) ; chr6:g.51912404A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51912404A>T , CM000668.2:g.51912404A>T	GRCh38
NC_000006.11:g.51777202A>T , CM000668.1:g.51777202A>T	GRCh37
NC_000006.10:g.51885161A>T	NCBI36
NG_008753.1:g.180222T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.6294T>A MANE Select	ENSP00000360158.3:p.Thr2098=
ENST00000340994.4:c.6294T>A	ENSP00000341097.4:p.Thr2098=
ENST00000371117.7:c.6294T>A	ENSP00000360158.3:p.Thr2098=
NM_138694.3:c.6294T>A	NP_619639.3:p.Thr2098=
NM_170724.2:c.6294T>A	NP_733842.2:p.Thr2098=
XM_011514679.1:c.6294T>A	XP_011512981.1:p.Thr2098=
XM_011514680.1:c.6294T>A	XP_011512982.1:p.Thr2098=
XM_011514681.1:c.6294T>A	XP_011512983.1:p.Thr2098=
XM_011514682.1:c.6294T>A	XP_011512984.1:p.Thr2098=
XM_011514683.1:c.5652T>A	XP_011512985.1:p.Thr1884=
XM_011514684.1:c.5583T>A	XP_011512986.1:p.Thr1861=
XM_011514685.1:c.6294T>A	XP_011512987.1:p.Thr2098=
XM_011514686.1:c.6294T>A	XP_011512988.1:p.Thr2098=
XM_011514687.1:c.6294T>A	XP_011512989.1:p.Thr2098=
XM_011514688.1:c.6294T>A	XP_011512990.1:p.Thr2098=
XM_011514689.1:c.6294T>A	XP_011512991.1:p.Thr2098=
XM_011514690.1:c.369T>A	XP_011512992.1:p.Thr123=
XM_011514691.1:c.369T>A	XP_011512993.1:p.Thr123=
XM_011514680.3:c.6294T>A	XP_011512982.1:p.Thr2098=
XM_011514682.3:c.6294T>A	XP_011512984.1:p.Thr2098=
XM_011514683.3:c.5652T>A	XP_011512985.1:p.Thr1884=
XM_011514684.3:c.5583T>A	XP_011512986.1:p.Thr1861=
XM_011514686.2:c.6294T>A	XP_011512988.1:p.Thr2098=
XM_011514688.2:c.6294T>A	XP_011512990.1:p.Thr2098=
XM_011514690.3:c.369T>A	XP_011512992.1:p.Thr123=
XM_011514691.3:c.369T>A	XP_011512993.1:p.Thr123=
XM_017010944.2:c.6294T>A	XP_016866433.1:p.Thr2098=
XM_017010945.2:c.6219T>A	XP_016866434.1:p.Thr2073=
XM_017010946.2:c.6294T>A	XP_016866435.1:p.Thr2098=
XM_017010947.2:c.6030T>A	XP_016866436.1:p.Thr2010=
XM_017010948.2:c.5583T>A	XP_016866437.1:p.Thr1861=
XM_017010949.2:c.4434T>A	XP_016866438.1:p.Thr1478=
XM_017010950.1:c.6294T>A	XP_016866439.1:p.Thr2098=
XM_017010951.1:c.6294T>A	XP_016866440.1:p.Thr2098=
XM_017010952.1:c.6294T>A	XP_016866441.1:p.Thr2098=
XR_001743469.1:n.6570T>A
NM_138694.4:c.6294T>A MANE Select	NP_619639.3:p.Thr2098=
NM_170724.3:c.6294T>A	NP_733842.2:p.Thr2098=