Canonical Allele Identifier: CA364431387

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524028T>A (hg19) ; chr6:g.51659230T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659230T>A , CM000668.2:g.51659230T>A	GRCh38
NC_000006.11:g.51524028T>A , CM000668.1:g.51524028T>A	GRCh37
NC_000006.10:g.51631987T>A	NCBI36
NG_008753.1:g.433396A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10896A>T MANE Select	ENSP00000360158.3:p.Arg3632Ser
ENST00000371117.7:c.10896A>T	ENSP00000360158.3:p.Arg3632Ser
NM_138694.3:c.10896A>T	NP_619639.3:p.Arg3632Ser
XM_011514679.1:c.10896A>T	XP_011512981.1:p.Arg3632Ser
XM_011514680.1:c.10896A>T	XP_011512982.1:p.Arg3632Ser
XM_011514681.1:c.10767A>T	XP_011512983.1:p.Arg3589Ser
XM_011514682.1:c.10758A>T	XP_011512984.1:p.Arg3586Ser
XM_011514683.1:c.10254A>T	XP_011512985.1:p.Arg3418Ser
XM_011514684.1:c.10185A>T	XP_011512986.1:p.Arg3395Ser
XM_011514687.1:c.10157-10010A>T	XP_011512989.1:n.10157-10010A>T
XM_011514690.1:c.4971A>T	XP_011512992.1:p.Arg1657Ser
XM_011514691.1:c.4971A>T	XP_011512993.1:p.Arg1657Ser
XR_926870.1:n.535+6857T>A
XR_926871.1:n.403+6857T>A
XR_926872.1:n.535+6857T>A
XM_011514680.3:c.10896A>T	XP_011512982.1:p.Arg3632Ser
XM_011514682.3:c.10758A>T	XP_011512984.1:p.Arg3586Ser
XM_011514683.3:c.10254A>T	XP_011512985.1:p.Arg3418Ser
XM_011514684.3:c.10185A>T	XP_011512986.1:p.Arg3395Ser
XM_011514690.3:c.4971A>T	XP_011512992.1:p.Arg1657Ser
XM_011514691.3:c.4971A>T	XP_011512993.1:p.Arg1657Ser
XM_017010944.2:c.10896A>T	XP_016866433.1:p.Arg3632Ser
XM_017010945.2:c.10821A>T	XP_016866434.1:p.Arg3607Ser
XM_017010946.2:c.10701A>T	XP_016866435.1:p.Arg3567Ser
XM_017010947.2:c.10632A>T	XP_016866436.1:p.Arg3544Ser
XM_017010948.2:c.10185A>T	XP_016866437.1:p.Arg3395Ser
XM_017010949.2:c.9036A>T	XP_016866438.1:p.Arg3012Ser
XR_001743469.1:n.11172A>T
XR_001744157.1:n.3145+6857T>A
XR_926870.2:n.3145+6857T>A
XR_926871.2:n.3013+6857T>A
XR_926872.2:n.3145+6857T>A
NM_138694.4:c.10896A>T MANE Select	NP_619639.3:p.Arg3632Ser