Canonical Allele Identifier: CA364418396

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491813C>A (hg19) ; chr6:g.51627015C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627015C>A , CM000668.2:g.51627015C>A	GRCh38
NC_000006.11:g.51491813C>A , CM000668.1:g.51491813C>A	GRCh37
NC_000006.10:g.51599772C>A	NCBI36
NG_008753.1:g.465611G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.11767G>T MANE Select	ENSP00000360158.3:p.Asp3923Tyr
ENST00000371117.7:c.11767G>T	ENSP00000360158.3:p.Asp3923Tyr
NM_138694.3:c.11767G>T	NP_619639.3:p.Asp3923Tyr
XM_011514679.1:c.11767G>T	XP_011512981.1:p.Asp3923Tyr
XM_011514680.1:c.11767G>T	XP_011512982.1:p.Asp3923Tyr
XM_011514681.1:c.11638G>T	XP_011512983.1:p.Asp3880Tyr
XM_011514682.1:c.11629G>T	XP_011512984.1:p.Asp3877Tyr
XM_011514683.1:c.11125G>T	XP_011512985.1:p.Asp3709Tyr
XM_011514684.1:c.11056G>T	XP_011512986.1:p.Asp3686Tyr
XM_011514690.1:c.5842G>T	XP_011512992.1:p.Asp1948Tyr
XM_011514691.1:c.5842G>T	XP_011512993.1:p.Asp1948Tyr
XM_011514680.3:c.11767G>T	XP_011512982.1:p.Asp3923Tyr
XM_011514682.3:c.11629G>T	XP_011512984.1:p.Asp3877Tyr
XM_011514683.3:c.11125G>T	XP_011512985.1:p.Asp3709Tyr
XM_011514684.3:c.11056G>T	XP_011512986.1:p.Asp3686Tyr
XM_011514690.3:c.5842G>T	XP_011512992.1:p.Asp1948Tyr
XM_011514691.3:c.5842G>T	XP_011512993.1:p.Asp1948Tyr
XM_017010944.2:c.11767G>T	XP_016866433.1:p.Asp3923Tyr
XM_017010945.2:c.11692G>T	XP_016866434.1:p.Asp3898Tyr
XM_017010946.2:c.11572G>T	XP_016866435.1:p.Asp3858Tyr
XM_017010947.2:c.11503G>T	XP_016866436.1:p.Asp3835Tyr
XM_017010948.2:c.11056G>T	XP_016866437.1:p.Asp3686Tyr
XM_017010949.2:c.9907G>T	XP_016866438.1:p.Asp3303Tyr
NM_138694.4:c.11767G>T MANE Select	NP_619639.3:p.Asp3923Tyr