Canonical Allele Identifier: CA364434044

Gene: PKHD1

Linked Data

• ClinVar Variation Id: 1074162
• ClinVar RCV Id: RCV001387380
• dbSNP Id: rs2150415240
• MyVariant Identifiers: chr6:g.51524363G>A (hg19) ; chr6:g.51659565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659565G>A , CM000668.2:g.51659565G>A	GRCh38
NC_000006.11:g.51524363G>A , CM000668.1:g.51524363G>A	GRCh37
NC_000006.10:g.51632322G>A	NCBI36
NG_008753.1:g.433061C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10561C>T MANE Select	ENSP00000360158.3:p.Gln3521Ter
ENST00000371117.7:c.10561C>T	ENSP00000360158.3:p.Gln3521Ter
NM_138694.3:c.10561C>T	NP_619639.3:p.Gln3521Ter
XM_011514679.1:c.10561C>T	XP_011512981.1:p.Gln3521Ter
XM_011514680.1:c.10561C>T	XP_011512982.1:p.Gln3521Ter
XM_011514681.1:c.10432C>T	XP_011512983.1:p.Gln3478Ter
XM_011514682.1:c.10423C>T	XP_011512984.1:p.Gln3475Ter
XM_011514683.1:c.9919C>T	XP_011512985.1:p.Gln3307Ter
XM_011514684.1:c.9850C>T	XP_011512986.1:p.Gln3284Ter
XM_011514687.1:c.10157-10345C>T	XP_011512989.1:n.10157-10345C>T
XM_011514690.1:c.4636C>T	XP_011512992.1:p.Gln1546Ter
XM_011514691.1:c.4636C>T	XP_011512993.1:p.Gln1546Ter
XR_926870.1:n.535+7192G>A
XR_926871.1:n.403+7192G>A
XR_926872.1:n.535+7192G>A
XM_011514680.3:c.10561C>T	XP_011512982.1:p.Gln3521Ter
XM_011514682.3:c.10423C>T	XP_011512984.1:p.Gln3475Ter
XM_011514683.3:c.9919C>T	XP_011512985.1:p.Gln3307Ter
XM_011514684.3:c.9850C>T	XP_011512986.1:p.Gln3284Ter
XM_011514690.3:c.4636C>T	XP_011512992.1:p.Gln1546Ter
XM_011514691.3:c.4636C>T	XP_011512993.1:p.Gln1546Ter
XM_017010944.2:c.10561C>T	XP_016866433.1:p.Gln3521Ter
XM_017010945.2:c.10486C>T	XP_016866434.1:p.Gln3496Ter
XM_017010946.2:c.10366C>T	XP_016866435.1:p.Gln3456Ter
XM_017010947.2:c.10297C>T	XP_016866436.1:p.Gln3433Ter
XM_017010948.2:c.9850C>T	XP_016866437.1:p.Gln3284Ter
XM_017010949.2:c.8701C>T	XP_016866438.1:p.Gln2901Ter
XR_001743469.1:n.10837C>T
XR_001744157.1:n.3145+7192G>A
XR_926870.2:n.3145+7192G>A
XR_926871.2:n.3013+7192G>A
XR_926872.2:n.3145+7192G>A
NM_138694.4:c.10561C>T MANE Select	NP_619639.3:p.Gln3521Ter