Canonical Allele Identifier: CA364418890

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491881G>C (hg19) ; chr6:g.51627083G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627083G>C , CM000668.2:g.51627083G>C	GRCh38
NC_000006.11:g.51491881G>C , CM000668.1:g.51491881G>C	GRCh37
NC_000006.10:g.51599840G>C	NCBI36
NG_008753.1:g.465543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11699C>G MANE Select	ENSP00000360158.3:p.Thr3900Ser
ENST00000371117.7:c.11699C>G	ENSP00000360158.3:p.Thr3900Ser
NM_138694.3:c.11699C>G	NP_619639.3:p.Thr3900Ser
XM_011514679.1:c.11699C>G	XP_011512981.1:p.Thr3900Ser
XM_011514680.1:c.11699C>G	XP_011512982.1:p.Thr3900Ser
XM_011514681.1:c.11570C>G	XP_011512983.1:p.Thr3857Ser
XM_011514682.1:c.11561C>G	XP_011512984.1:p.Thr3854Ser
XM_011514683.1:c.11057C>G	XP_011512985.1:p.Thr3686Ser
XM_011514684.1:c.10988C>G	XP_011512986.1:p.Thr3663Ser
XM_011514690.1:c.5774C>G	XP_011512992.1:p.Thr1925Ser
XM_011514691.1:c.5774C>G	XP_011512993.1:p.Thr1925Ser
XM_011514680.3:c.11699C>G	XP_011512982.1:p.Thr3900Ser
XM_011514682.3:c.11561C>G	XP_011512984.1:p.Thr3854Ser
XM_011514683.3:c.11057C>G	XP_011512985.1:p.Thr3686Ser
XM_011514684.3:c.10988C>G	XP_011512986.1:p.Thr3663Ser
XM_011514690.3:c.5774C>G	XP_011512992.1:p.Thr1925Ser
XM_011514691.3:c.5774C>G	XP_011512993.1:p.Thr1925Ser
XM_017010944.2:c.11699C>G	XP_016866433.1:p.Thr3900Ser
XM_017010945.2:c.11624C>G	XP_016866434.1:p.Thr3875Ser
XM_017010946.2:c.11504C>G	XP_016866435.1:p.Thr3835Ser
XM_017010947.2:c.11435C>G	XP_016866436.1:p.Thr3812Ser
XM_017010948.2:c.10988C>G	XP_016866437.1:p.Thr3663Ser
XM_017010949.2:c.9839C>G	XP_016866438.1:p.Thr3280Ser
NM_138694.4:c.11699C>G MANE Select	NP_619639.3:p.Thr3900Ser