Canonical Allele Identifier: CA364424089

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 1362666
• ClinVar RCV Id: RCV001934528
• dbSNP Id: rs2150987139
• MyVariant Identifiers: chr6:g.51613370A>C (hg19) ; chr6:g.51748572A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748572A>C , CM000668.2:g.51748572A>C	GRCh38
NC_000006.11:g.51613370A>C , CM000668.1:g.51613370A>C	GRCh37
NC_000006.10:g.51721329A>C	NCBI36
NG_008753.1:g.344054T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.9044T>G MANE Select	ENSP00000360158.3:p.Ile3015Ser
ENST00000340994.4:c.9044T>G	ENSP00000341097.4:p.Ile3015Ser
ENST00000371117.7:c.9044T>G	ENSP00000360158.3:p.Ile3015Ser
NM_138694.3:c.9044T>G	NP_619639.3:p.Ile3015Ser
NM_170724.2:c.9044T>G	NP_733842.2:p.Ile3015Ser
XM_011514679.1:c.9044T>G	XP_011512981.1:p.Ile3015Ser
XM_011514680.1:c.9044T>G	XP_011512982.1:p.Ile3015Ser
XM_011514681.1:c.8915T>G	XP_011512983.1:p.Ile2972Ser
XM_011514682.1:c.8906T>G	XP_011512984.1:p.Ile2969Ser
XM_011514683.1:c.8402T>G	XP_011512985.1:p.Ile2801Ser
XM_011514684.1:c.8333T>G	XP_011512986.1:p.Ile2778Ser
XM_011514685.1:c.9044T>G	XP_011512987.1:p.Ile3015Ser
XM_011514686.1:c.9044T>G	XP_011512988.1:p.Ile3015Ser
XM_011514687.1:c.9044T>G	XP_011512989.1:p.Ile3015Ser
XM_011514688.1:c.9044T>G	XP_011512990.1:p.Ile3015Ser
XM_011514690.1:c.3119T>G	XP_011512992.1:p.Ile1040Ser
XM_011514691.1:c.3119T>G	XP_011512993.1:p.Ile1040Ser
XM_011514680.3:c.9044T>G	XP_011512982.1:p.Ile3015Ser
XM_011514682.3:c.8906T>G	XP_011512984.1:p.Ile2969Ser
XM_011514683.3:c.8402T>G	XP_011512985.1:p.Ile2801Ser
XM_011514684.3:c.8333T>G	XP_011512986.1:p.Ile2778Ser
XM_011514686.2:c.9044T>G	XP_011512988.1:p.Ile3015Ser
XM_011514688.2:c.9044T>G	XP_011512990.1:p.Ile3015Ser
XM_011514690.3:c.3119T>G	XP_011512992.1:p.Ile1040Ser
XM_011514691.3:c.3119T>G	XP_011512993.1:p.Ile1040Ser
XM_017010944.2:c.9044T>G	XP_016866433.1:p.Ile3015Ser
XM_017010945.2:c.8969T>G	XP_016866434.1:p.Ile2990Ser
XM_017010946.2:c.8849T>G	XP_016866435.1:p.Ile2950Ser
XM_017010947.2:c.8780T>G	XP_016866436.1:p.Ile2927Ser
XM_017010948.2:c.8333T>G	XP_016866437.1:p.Ile2778Ser
XM_017010949.2:c.7184T>G	XP_016866438.1:p.Ile2395Ser
XM_017010950.1:c.9044T>G	XP_016866439.1:p.Ile3015Ser
XR_001743469.1:n.9320T>G
NM_138694.4:c.9044T>G MANE Select	NP_619639.3:p.Ile3015Ser
NM_170724.3:c.9044T>G	NP_733842.2:p.Ile3015Ser