Canonical Allele Identifier: CA450614030

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51613378T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748580T>A , CM000668.2:g.51748580T>A	GRCh38
NC_000006.11:g.51613378T>A , CM000668.1:g.51613378T>A	GRCh37
NC_000006.10:g.51721337T>A	NCBI36
NG_008753.1:g.344046A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.9036A>T MANE Select	ENSP00000360158.3:p.Gly3012=
ENST00000340994.4:c.9036A>T	ENSP00000341097.4:p.Gly3012=
ENST00000371117.7:c.9036A>T	ENSP00000360158.3:p.Gly3012=
NM_138694.3:c.9036A>T	NP_619639.3:p.Gly3012=
NM_170724.2:c.9036A>T	NP_733842.2:p.Gly3012=
XM_011514679.1:c.9036A>T	XP_011512981.1:p.Gly3012=
XM_011514680.1:c.9036A>T	XP_011512982.1:p.Gly3012=
XM_011514681.1:c.8907A>T	XP_011512983.1:p.Gly2969=
XM_011514682.1:c.8898A>T	XP_011512984.1:p.Gly2966=
XM_011514683.1:c.8394A>T	XP_011512985.1:p.Gly2798=
XM_011514684.1:c.8325A>T	XP_011512986.1:p.Gly2775=
XM_011514685.1:c.9036A>T	XP_011512987.1:p.Gly3012=
XM_011514686.1:c.9036A>T	XP_011512988.1:p.Gly3012=
XM_011514687.1:c.9036A>T	XP_011512989.1:p.Gly3012=
XM_011514688.1:c.9036A>T	XP_011512990.1:p.Gly3012=
XM_011514690.1:c.3111A>T	XP_011512992.1:p.Gly1037=
XM_011514691.1:c.3111A>T	XP_011512993.1:p.Gly1037=
XM_011514680.3:c.9036A>T	XP_011512982.1:p.Gly3012=
XM_011514682.3:c.8898A>T	XP_011512984.1:p.Gly2966=
XM_011514683.3:c.8394A>T	XP_011512985.1:p.Gly2798=
XM_011514684.3:c.8325A>T	XP_011512986.1:p.Gly2775=
XM_011514686.2:c.9036A>T	XP_011512988.1:p.Gly3012=
XM_011514688.2:c.9036A>T	XP_011512990.1:p.Gly3012=
XM_011514690.3:c.3111A>T	XP_011512992.1:p.Gly1037=
XM_011514691.3:c.3111A>T	XP_011512993.1:p.Gly1037=
XM_017010944.2:c.9036A>T	XP_016866433.1:p.Gly3012=
XM_017010945.2:c.8961A>T	XP_016866434.1:p.Gly2987=
XM_017010946.2:c.8841A>T	XP_016866435.1:p.Gly2947=
XM_017010947.2:c.8772A>T	XP_016866436.1:p.Gly2924=
XM_017010948.2:c.8325A>T	XP_016866437.1:p.Gly2775=
XM_017010949.2:c.7176A>T	XP_016866438.1:p.Gly2392=
XM_017010950.1:c.9036A>T	XP_016866439.1:p.Gly3012=
XR_001743469.1:n.9312A>T
NM_138694.4:c.9036A>T MANE Select	NP_619639.3:p.Gly3012=
NM_170724.3:c.9036A>T	NP_733842.2:p.Gly3012=