Canonical Allele Identifier: CA10624391

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 357396
• ClinVar RCV Id: RCV000315066
• dbSNP Id: rs886061607
• MyVariant Identifiers: chr6:g.51483119A>C (hg19) ; chr6:g.51618321A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51618321A>C , CM000668.2:g.51618321A>C	GRCh38
NC_000006.11:g.51483119A>C , CM000668.1:g.51483119A>C	GRCh37
NC_000006.10:g.51591078A>C	NCBI36
NG_008753.1:g.474305T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.*760T>G MANE Select	ENSP00000360158.3:n.*760T>G
ENST00000371117.7:c.*760T>G	ENSP00000360158.3:n.*760T>G
NM_138694.3:c.*760T>G	NP_619639.3:n.*760T>G
XM_011514679.1:c.*760T>G	XP_011512981.1:n.*760T>G
XM_011514680.1:c.*760T>G	XP_011512982.1:n.*760T>G
XM_011514681.1:c.*760T>G	XP_011512983.1:n.*760T>G
XM_011514682.1:c.*760T>G	XP_011512984.1:n.*760T>G
XM_011514683.1:c.*760T>G	XP_011512985.1:n.*760T>G
XM_011514684.1:c.*760T>G	XP_011512986.1:n.*760T>G
XM_011514690.1:c.*760T>G	XP_011512992.1:n.*760T>G
XM_011514691.1:c.*760T>G	XP_011512993.1:n.*760T>G
XM_011514680.3:c.*760T>G	XP_011512982.1:n.*760T>G
XM_011514682.3:c.*760T>G	XP_011512984.1:n.*760T>G
XM_011514683.3:c.*760T>G	XP_011512985.1:n.*760T>G
XM_011514684.3:c.*760T>G	XP_011512986.1:n.*760T>G
XM_011514690.3:c.*760T>G	XP_011512992.1:n.*760T>G
XM_011514691.3:c.*760T>G	XP_011512993.1:n.*760T>G
XM_017010944.2:c.*760T>G	XP_016866433.1:n.*760T>G
XM_017010945.2:c.*760T>G	XP_016866434.1:n.*760T>G
XM_017010946.2:c.*760T>G	XP_016866435.1:n.*760T>G
XM_017010947.2:c.*760T>G	XP_016866436.1:n.*760T>G
XM_017010948.2:c.*760T>G	XP_016866437.1:n.*760T>G
XM_017010949.2:c.*760T>G	XP_016866438.1:n.*760T>G
NM_138694.4:c.*760T>G MANE Select	NP_619639.3:n.*760T>G