Canonical Allele Identifier: CA364436538

Gene: PKHD1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10301C>G MANE Select	ENSP00000360158.3:p.Thr3434Ser
ENST00000371117.7:c.10301C>G	ENSP00000360158.3:p.Thr3434Ser
NM_138694.3:c.10301C>G	NP_619639.3:p.Thr3434Ser
XM_011514679.1:c.10301C>G	XP_011512981.1:p.Thr3434Ser
XM_011514680.1:c.10301C>G	XP_011512982.1:p.Thr3434Ser
XM_011514681.1:c.10172C>G	XP_011512983.1:p.Thr3391Ser
XM_011514682.1:c.10163C>G	XP_011512984.1:p.Thr3388Ser
XM_011514683.1:c.9659C>G	XP_011512985.1:p.Thr3220Ser
XM_011514684.1:c.9590C>G	XP_011512986.1:p.Thr3197Ser
XM_011514687.1:c.10157-10605C>G	XP_011512989.1:n.10157-10605C>G
XM_011514690.1:c.4376C>G	XP_011512992.1:p.Thr1459Ser
XM_011514691.1:c.4376C>G	XP_011512993.1:p.Thr1459Ser
XR_926870.1:n.535+7452G>C
XR_926871.1:n.403+7452G>C
XR_926872.1:n.535+7452G>C
XM_011514680.3:c.10301C>G	XP_011512982.1:p.Thr3434Ser
XM_011514682.3:c.10163C>G	XP_011512984.1:p.Thr3388Ser
XM_011514683.3:c.9659C>G	XP_011512985.1:p.Thr3220Ser
XM_011514684.3:c.9590C>G	XP_011512986.1:p.Thr3197Ser
XM_011514690.3:c.4376C>G	XP_011512992.1:p.Thr1459Ser
XM_011514691.3:c.4376C>G	XP_011512993.1:p.Thr1459Ser
XM_017010944.2:c.10301C>G	XP_016866433.1:p.Thr3434Ser
XM_017010945.2:c.10226C>G	XP_016866434.1:p.Thr3409Ser
XM_017010946.2:c.10106C>G	XP_016866435.1:p.Thr3369Ser
XM_017010947.2:c.10037C>G	XP_016866436.1:p.Thr3346Ser
XM_017010948.2:c.9590C>G	XP_016866437.1:p.Thr3197Ser
XM_017010949.2:c.8441C>G	XP_016866438.1:p.Thr2814Ser
XR_001743469.1:n.10577C>G
XR_001744157.1:n.3145+7452G>C
XR_926870.2:n.3145+7452G>C
XR_926871.2:n.3013+7452G>C
XR_926872.2:n.3145+7452G>C
NM_138694.4:c.10301C>G MANE Select	NP_619639.3:p.Thr3434Ser