Canonical Allele Identifier: CA450411475

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491796T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51626998T>C , CM000668.2:g.51626998T>C	GRCh38
NC_000006.11:g.51491796T>C , CM000668.1:g.51491796T>C	GRCh37
NC_000006.10:g.51599755T>C	NCBI36
NG_008753.1:g.465628A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11784A>G MANE Select	ENSP00000360158.3:p.Glu3928=
ENST00000371117.7:c.11784A>G	ENSP00000360158.3:p.Glu3928=
NM_138694.3:c.11784A>G	NP_619639.3:p.Glu3928=
XM_011514679.1:c.11784A>G	XP_011512981.1:p.Glu3928=
XM_011514680.1:c.11784A>G	XP_011512982.1:p.Glu3928=
XM_011514681.1:c.11655A>G	XP_011512983.1:p.Glu3885=
XM_011514682.1:c.11646A>G	XP_011512984.1:p.Glu3882=
XM_011514683.1:c.11142A>G	XP_011512985.1:p.Glu3714=
XM_011514684.1:c.11073A>G	XP_011512986.1:p.Glu3691=
XM_011514690.1:c.5859A>G	XP_011512992.1:p.Glu1953=
XM_011514691.1:c.5859A>G	XP_011512993.1:p.Glu1953=
XM_011514680.3:c.11784A>G	XP_011512982.1:p.Glu3928=
XM_011514682.3:c.11646A>G	XP_011512984.1:p.Glu3882=
XM_011514683.3:c.11142A>G	XP_011512985.1:p.Glu3714=
XM_011514684.3:c.11073A>G	XP_011512986.1:p.Glu3691=
XM_011514690.3:c.5859A>G	XP_011512992.1:p.Glu1953=
XM_011514691.3:c.5859A>G	XP_011512993.1:p.Glu1953=
XM_017010944.2:c.11784A>G	XP_016866433.1:p.Glu3928=
XM_017010945.2:c.11709A>G	XP_016866434.1:p.Glu3903=
XM_017010946.2:c.11589A>G	XP_016866435.1:p.Glu3863=
XM_017010947.2:c.11520A>G	XP_016866436.1:p.Glu3840=
XM_017010948.2:c.11073A>G	XP_016866437.1:p.Glu3691=
XM_017010949.2:c.9924A>G	XP_016866438.1:p.Glu3308=
NM_138694.4:c.11784A>G MANE Select	NP_619639.3:p.Glu3928=