Canonical Allele Identifier: CA364418352

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491806A>G (hg19) ; chr6:g.51627008A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627008A>G , CM000668.2:g.51627008A>G	GRCh38
NC_000006.11:g.51491806A>G , CM000668.1:g.51491806A>G	GRCh37
NC_000006.10:g.51599765A>G	NCBI36
NG_008753.1:g.465618T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.11774T>C MANE Select	ENSP00000360158.3:p.Val3925Ala
ENST00000371117.7:c.11774T>C	ENSP00000360158.3:p.Val3925Ala
NM_138694.3:c.11774T>C	NP_619639.3:p.Val3925Ala
XM_011514679.1:c.11774T>C	XP_011512981.1:p.Val3925Ala
XM_011514680.1:c.11774T>C	XP_011512982.1:p.Val3925Ala
XM_011514681.1:c.11645T>C	XP_011512983.1:p.Val3882Ala
XM_011514682.1:c.11636T>C	XP_011512984.1:p.Val3879Ala
XM_011514683.1:c.11132T>C	XP_011512985.1:p.Val3711Ala
XM_011514684.1:c.11063T>C	XP_011512986.1:p.Val3688Ala
XM_011514690.1:c.5849T>C	XP_011512992.1:p.Val1950Ala
XM_011514691.1:c.5849T>C	XP_011512993.1:p.Val1950Ala
XM_011514680.3:c.11774T>C	XP_011512982.1:p.Val3925Ala
XM_011514682.3:c.11636T>C	XP_011512984.1:p.Val3879Ala
XM_011514683.3:c.11132T>C	XP_011512985.1:p.Val3711Ala
XM_011514684.3:c.11063T>C	XP_011512986.1:p.Val3688Ala
XM_011514690.3:c.5849T>C	XP_011512992.1:p.Val1950Ala
XM_011514691.3:c.5849T>C	XP_011512993.1:p.Val1950Ala
XM_017010944.2:c.11774T>C	XP_016866433.1:p.Val3925Ala
XM_017010945.2:c.11699T>C	XP_016866434.1:p.Val3900Ala
XM_017010946.2:c.11579T>C	XP_016866435.1:p.Val3860Ala
XM_017010947.2:c.11510T>C	XP_016866436.1:p.Val3837Ala
XM_017010948.2:c.11063T>C	XP_016866437.1:p.Val3688Ala
XM_017010949.2:c.9914T>C	XP_016866438.1:p.Val3305Ala
NM_138694.4:c.11774T>C MANE Select	NP_619639.3:p.Val3925Ala