Canonical Allele Identifier: CA364431636

Gene: PKHD1

Linked Data

• dbSNP Id: rs1562040858
• gnomAD v3: 6-51659279-G-T
• gnomAD v4: 6-51659279-G-T
• MyVariant Identifiers: chr6:g.51524077G>T (hg19) ; chr6:g.51659279G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659279G>T , CM000668.2:g.51659279G>T	GRCh38
NC_000006.11:g.51524077G>T , CM000668.1:g.51524077G>T	GRCh37
NC_000006.10:g.51632036G>T	NCBI36
NG_008753.1:g.433347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10847C>A MANE Select	ENSP00000360158.3:p.Ala3616Glu
ENST00000371117.7:c.10847C>A	ENSP00000360158.3:p.Ala3616Glu
NM_138694.3:c.10847C>A	NP_619639.3:p.Ala3616Glu
XM_011514679.1:c.10847C>A	XP_011512981.1:p.Ala3616Glu
XM_011514680.1:c.10847C>A	XP_011512982.1:p.Ala3616Glu
XM_011514681.1:c.10718C>A	XP_011512983.1:p.Ala3573Glu
XM_011514682.1:c.10709C>A	XP_011512984.1:p.Ala3570Glu
XM_011514683.1:c.10205C>A	XP_011512985.1:p.Ala3402Glu
XM_011514684.1:c.10136C>A	XP_011512986.1:p.Ala3379Glu
XM_011514687.1:c.10157-10059C>A	XP_011512989.1:n.10157-10059C>A
XM_011514690.1:c.4922C>A	XP_011512992.1:p.Ala1641Glu
XM_011514691.1:c.4922C>A	XP_011512993.1:p.Ala1641Glu
XR_926870.1:n.535+6906G>T
XR_926871.1:n.403+6906G>T
XR_926872.1:n.535+6906G>T
XM_011514680.3:c.10847C>A	XP_011512982.1:p.Ala3616Glu
XM_011514682.3:c.10709C>A	XP_011512984.1:p.Ala3570Glu
XM_011514683.3:c.10205C>A	XP_011512985.1:p.Ala3402Glu
XM_011514684.3:c.10136C>A	XP_011512986.1:p.Ala3379Glu
XM_011514690.3:c.4922C>A	XP_011512992.1:p.Ala1641Glu
XM_011514691.3:c.4922C>A	XP_011512993.1:p.Ala1641Glu
XM_017010944.2:c.10847C>A	XP_016866433.1:p.Ala3616Glu
XM_017010945.2:c.10772C>A	XP_016866434.1:p.Ala3591Glu
XM_017010946.2:c.10652C>A	XP_016866435.1:p.Ala3551Glu
XM_017010947.2:c.10583C>A	XP_016866436.1:p.Ala3528Glu
XM_017010948.2:c.10136C>A	XP_016866437.1:p.Ala3379Glu
XM_017010949.2:c.8987C>A	XP_016866438.1:p.Ala2996Glu
XR_001743469.1:n.11123C>A
XR_001744157.1:n.3145+6906G>T
XR_926870.2:n.3145+6906G>T
XR_926871.2:n.3013+6906G>T
XR_926872.2:n.3145+6906G>T
NM_138694.4:c.10847C>A MANE Select	NP_619639.3:p.Ala3616Glu