Canonical Allele Identifier: CA364418768

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491853G>C (hg19) ; chr6:g.51627055G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627055G>C , CM000668.2:g.51627055G>C	GRCh38
NC_000006.11:g.51491853G>C , CM000668.1:g.51491853G>C	GRCh37
NC_000006.10:g.51599812G>C	NCBI36
NG_008753.1:g.465571C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11727C>G MANE Select	ENSP00000360158.3:p.Ile3909Met
ENST00000371117.7:c.11727C>G	ENSP00000360158.3:p.Ile3909Met
NM_138694.3:c.11727C>G	NP_619639.3:p.Ile3909Met
XM_011514679.1:c.11727C>G	XP_011512981.1:p.Ile3909Met
XM_011514680.1:c.11727C>G	XP_011512982.1:p.Ile3909Met
XM_011514681.1:c.11598C>G	XP_011512983.1:p.Ile3866Met
XM_011514682.1:c.11589C>G	XP_011512984.1:p.Ile3863Met
XM_011514683.1:c.11085C>G	XP_011512985.1:p.Ile3695Met
XM_011514684.1:c.11016C>G	XP_011512986.1:p.Ile3672Met
XM_011514690.1:c.5802C>G	XP_011512992.1:p.Ile1934Met
XM_011514691.1:c.5802C>G	XP_011512993.1:p.Ile1934Met
XM_011514680.3:c.11727C>G	XP_011512982.1:p.Ile3909Met
XM_011514682.3:c.11589C>G	XP_011512984.1:p.Ile3863Met
XM_011514683.3:c.11085C>G	XP_011512985.1:p.Ile3695Met
XM_011514684.3:c.11016C>G	XP_011512986.1:p.Ile3672Met
XM_011514690.3:c.5802C>G	XP_011512992.1:p.Ile1934Met
XM_011514691.3:c.5802C>G	XP_011512993.1:p.Ile1934Met
XM_017010944.2:c.11727C>G	XP_016866433.1:p.Ile3909Met
XM_017010945.2:c.11652C>G	XP_016866434.1:p.Ile3884Met
XM_017010946.2:c.11532C>G	XP_016866435.1:p.Ile3844Met
XM_017010947.2:c.11463C>G	XP_016866436.1:p.Ile3821Met
XM_017010948.2:c.11016C>G	XP_016866437.1:p.Ile3672Met
XM_017010949.2:c.9867C>G	XP_016866438.1:p.Ile3289Met
NM_138694.4:c.11727C>G MANE Select	NP_619639.3:p.Ile3909Met