Canonical Allele Identifier: CA364419748

Gene: PKHD1

Linked Data

• dbSNP Id: rs2150974867
• MyVariant Identifiers: chr6:g.51611669A>G (hg19) ; chr6:g.51746871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51746871A>G , CM000668.2:g.51746871A>G	GRCh38
NC_000006.11:g.51611669A>G , CM000668.1:g.51611669A>G	GRCh37
NC_000006.10:g.51719628A>G	NCBI36
NG_008753.1:g.345755T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.9848T>C MANE Select	ENSP00000360158.3:p.Phe3283Ser
ENST00000340994.4:c.9848T>C	ENSP00000341097.4:p.Phe3283Ser
ENST00000371117.7:c.9848T>C	ENSP00000360158.3:p.Phe3283Ser
NM_138694.3:c.9848T>C	NP_619639.3:p.Phe3283Ser
NM_170724.2:c.9848T>C	NP_733842.2:p.Phe3283Ser
XM_011514679.1:c.9848T>C	XP_011512981.1:p.Phe3283Ser
XM_011514680.1:c.9848T>C	XP_011512982.1:p.Phe3283Ser
XM_011514681.1:c.9719T>C	XP_011512983.1:p.Phe3240Ser
XM_011514682.1:c.9710T>C	XP_011512984.1:p.Phe3237Ser
XM_011514683.1:c.9206T>C	XP_011512985.1:p.Phe3069Ser
XM_011514684.1:c.9137T>C	XP_011512986.1:p.Phe3046Ser
XM_011514685.1:c.9848T>C	XP_011512987.1:p.Phe3283Ser
XM_011514686.1:c.9848T>C	XP_011512988.1:p.Phe3283Ser
XM_011514687.1:c.9848T>C	XP_011512989.1:p.Phe3283Ser
XM_011514688.1:c.9832T>C	XP_011512990.1:p.Leu3278=
XM_011514690.1:c.3923T>C	XP_011512992.1:p.Phe1308Ser
XM_011514691.1:c.3923T>C	XP_011512993.1:p.Phe1308Ser
XM_011514680.3:c.9848T>C	XP_011512982.1:p.Phe3283Ser
XM_011514682.3:c.9710T>C	XP_011512984.1:p.Phe3237Ser
XM_011514683.3:c.9206T>C	XP_011512985.1:p.Phe3069Ser
XM_011514684.3:c.9137T>C	XP_011512986.1:p.Phe3046Ser
XM_011514686.2:c.9848T>C	XP_011512988.1:p.Phe3283Ser
XM_011514688.2:c.9832T>C	XP_011512990.1:p.Leu3278=
XM_011514690.3:c.3923T>C	XP_011512992.1:p.Phe1308Ser
XM_011514691.3:c.3923T>C	XP_011512993.1:p.Phe1308Ser
XM_017010944.2:c.9848T>C	XP_016866433.1:p.Phe3283Ser
XM_017010945.2:c.9773T>C	XP_016866434.1:p.Phe3258Ser
XM_017010946.2:c.9653T>C	XP_016866435.1:p.Phe3218Ser
XM_017010947.2:c.9584T>C	XP_016866436.1:p.Phe3195Ser
XM_017010948.2:c.9137T>C	XP_016866437.1:p.Phe3046Ser
XM_017010949.2:c.7988T>C	XP_016866438.1:p.Phe2663Ser
XM_017010950.1:c.9848T>C	XP_016866439.1:p.Phe3283Ser
XR_001743469.1:n.10124T>C
NM_138694.4:c.9848T>C MANE Select	NP_619639.3:p.Phe3283Ser
NM_170724.3:c.9848T>C	NP_733842.2:p.Phe3283Ser