Canonical Allele Identifier: CA364436534

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524623G>A (hg19) ; chr6:g.51659825G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659825G>A , CM000668.2:g.51659825G>A	GRCh38
NC_000006.11:g.51524623G>A , CM000668.1:g.51524623G>A	GRCh37
NC_000006.10:g.51632582G>A	NCBI36
NG_008753.1:g.432801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10301C>T MANE Select	ENSP00000360158.3:p.Thr3434Ile
ENST00000371117.7:c.10301C>T	ENSP00000360158.3:p.Thr3434Ile
NM_138694.3:c.10301C>T	NP_619639.3:p.Thr3434Ile
XM_011514679.1:c.10301C>T	XP_011512981.1:p.Thr3434Ile
XM_011514680.1:c.10301C>T	XP_011512982.1:p.Thr3434Ile
XM_011514681.1:c.10172C>T	XP_011512983.1:p.Thr3391Ile
XM_011514682.1:c.10163C>T	XP_011512984.1:p.Thr3388Ile
XM_011514683.1:c.9659C>T	XP_011512985.1:p.Thr3220Ile
XM_011514684.1:c.9590C>T	XP_011512986.1:p.Thr3197Ile
XM_011514687.1:c.10157-10605C>T	XP_011512989.1:n.10157-10605C>T
XM_011514690.1:c.4376C>T	XP_011512992.1:p.Thr1459Ile
XM_011514691.1:c.4376C>T	XP_011512993.1:p.Thr1459Ile
XR_926870.1:n.535+7452G>A
XR_926871.1:n.403+7452G>A
XR_926872.1:n.535+7452G>A
XM_011514680.3:c.10301C>T	XP_011512982.1:p.Thr3434Ile
XM_011514682.3:c.10163C>T	XP_011512984.1:p.Thr3388Ile
XM_011514683.3:c.9659C>T	XP_011512985.1:p.Thr3220Ile
XM_011514684.3:c.9590C>T	XP_011512986.1:p.Thr3197Ile
XM_011514690.3:c.4376C>T	XP_011512992.1:p.Thr1459Ile
XM_011514691.3:c.4376C>T	XP_011512993.1:p.Thr1459Ile
XM_017010944.2:c.10301C>T	XP_016866433.1:p.Thr3434Ile
XM_017010945.2:c.10226C>T	XP_016866434.1:p.Thr3409Ile
XM_017010946.2:c.10106C>T	XP_016866435.1:p.Thr3369Ile
XM_017010947.2:c.10037C>T	XP_016866436.1:p.Thr3346Ile
XM_017010948.2:c.9590C>T	XP_016866437.1:p.Thr3197Ile
XM_017010949.2:c.8441C>T	XP_016866438.1:p.Thr2814Ile
XR_001743469.1:n.10577C>T
XR_001744157.1:n.3145+7452G>A
XR_926870.2:n.3145+7452G>A
XR_926871.2:n.3013+7452G>A
XR_926872.2:n.3145+7452G>A
NM_138694.4:c.10301C>T MANE Select	NP_619639.3:p.Thr3434Ile