Canonical Allele Identifier: CA364437516

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524740G>C (hg19) ; chr6:g.51659942G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659942G>C , CM000668.2:g.51659942G>C	GRCh38
NC_000006.11:g.51524740G>C , CM000668.1:g.51524740G>C	GRCh37
NC_000006.10:g.51632699G>C	NCBI36
NG_008753.1:g.432684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10184C>G MANE Select	ENSP00000360158.3:p.Thr3395Arg
ENST00000371117.7:c.10184C>G	ENSP00000360158.3:p.Thr3395Arg
NM_138694.3:c.10184C>G	NP_619639.3:p.Thr3395Arg
XM_011514679.1:c.10184C>G	XP_011512981.1:p.Thr3395Arg
XM_011514680.1:c.10184C>G	XP_011512982.1:p.Thr3395Arg
XM_011514681.1:c.10055C>G	XP_011512983.1:p.Thr3352Arg
XM_011514682.1:c.10046C>G	XP_011512984.1:p.Thr3349Arg
XM_011514683.1:c.9542C>G	XP_011512985.1:p.Thr3181Arg
XM_011514684.1:c.9473C>G	XP_011512986.1:p.Thr3158Arg
XM_011514687.1:c.10157-10722C>G	XP_011512989.1:n.10157-10722C>G
XM_011514690.1:c.4259C>G	XP_011512992.1:p.Thr1420Arg
XM_011514691.1:c.4259C>G	XP_011512993.1:p.Thr1420Arg
XR_926870.1:n.535+7569G>C
XR_926871.1:n.403+7569G>C
XR_926872.1:n.535+7569G>C
XM_011514680.3:c.10184C>G	XP_011512982.1:p.Thr3395Arg
XM_011514682.3:c.10046C>G	XP_011512984.1:p.Thr3349Arg
XM_011514683.3:c.9542C>G	XP_011512985.1:p.Thr3181Arg
XM_011514684.3:c.9473C>G	XP_011512986.1:p.Thr3158Arg
XM_011514690.3:c.4259C>G	XP_011512992.1:p.Thr1420Arg
XM_011514691.3:c.4259C>G	XP_011512993.1:p.Thr1420Arg
XM_017010944.2:c.10184C>G	XP_016866433.1:p.Thr3395Arg
XM_017010945.2:c.10109C>G	XP_016866434.1:p.Thr3370Arg
XM_017010946.2:c.9989C>G	XP_016866435.1:p.Thr3330Arg
XM_017010947.2:c.9920C>G	XP_016866436.1:p.Thr3307Arg
XM_017010948.2:c.9473C>G	XP_016866437.1:p.Thr3158Arg
XM_017010949.2:c.8324C>G	XP_016866438.1:p.Thr2775Arg
XR_001743469.1:n.10460C>G
XR_001744157.1:n.3145+7569G>C
XR_926870.2:n.3145+7569G>C
XR_926871.2:n.3013+7569G>C
XR_926872.2:n.3145+7569G>C
NM_138694.4:c.10184C>G MANE Select	NP_619639.3:p.Thr3395Arg