Canonical Allele Identifier: CA364431257

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524002A>C (hg19) ; chr6:g.51659204A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659204A>C , CM000668.2:g.51659204A>C	GRCh38
NC_000006.11:g.51524002A>C , CM000668.1:g.51524002A>C	GRCh37
NC_000006.10:g.51631961A>C	NCBI36
NG_008753.1:g.433422T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10922T>G MANE Select	ENSP00000360158.3:p.Met3641Arg
ENST00000371117.7:c.10922T>G	ENSP00000360158.3:p.Met3641Arg
NM_138694.3:c.10922T>G	NP_619639.3:p.Met3641Arg
XM_011514679.1:c.10922T>G	XP_011512981.1:p.Met3641Arg
XM_011514680.1:c.10922T>G	XP_011512982.1:p.Met3641Arg
XM_011514681.1:c.10793T>G	XP_011512983.1:p.Met3598Arg
XM_011514682.1:c.10784T>G	XP_011512984.1:p.Met3595Arg
XM_011514683.1:c.10280T>G	XP_011512985.1:p.Met3427Arg
XM_011514684.1:c.10211T>G	XP_011512986.1:p.Met3404Arg
XM_011514687.1:c.10157-9984T>G	XP_011512989.1:n.10157-9984T>G
XM_011514690.1:c.4997T>G	XP_011512992.1:p.Met1666Arg
XM_011514691.1:c.4997T>G	XP_011512993.1:p.Met1666Arg
XR_926870.1:n.535+6831A>C
XR_926871.1:n.403+6831A>C
XR_926872.1:n.535+6831A>C
XM_011514680.3:c.10922T>G	XP_011512982.1:p.Met3641Arg
XM_011514682.3:c.10784T>G	XP_011512984.1:p.Met3595Arg
XM_011514683.3:c.10280T>G	XP_011512985.1:p.Met3427Arg
XM_011514684.3:c.10211T>G	XP_011512986.1:p.Met3404Arg
XM_011514690.3:c.4997T>G	XP_011512992.1:p.Met1666Arg
XM_011514691.3:c.4997T>G	XP_011512993.1:p.Met1666Arg
XM_017010944.2:c.10922T>G	XP_016866433.1:p.Met3641Arg
XM_017010945.2:c.10847T>G	XP_016866434.1:p.Met3616Arg
XM_017010946.2:c.10727T>G	XP_016866435.1:p.Met3576Arg
XM_017010947.2:c.10658T>G	XP_016866436.1:p.Met3553Arg
XM_017010948.2:c.10211T>G	XP_016866437.1:p.Met3404Arg
XM_017010949.2:c.9062T>G	XP_016866438.1:p.Met3021Arg
XR_001743469.1:n.11198T>G
XR_001744157.1:n.3145+6831A>C
XR_926870.2:n.3145+6831A>C
XR_926871.2:n.3013+6831A>C
XR_926872.2:n.3145+6831A>C
NM_138694.4:c.10922T>G MANE Select	NP_619639.3:p.Met3641Arg