Canonical Allele Identifier: CA450411507

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491823G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627025G>A , CM000668.2:g.51627025G>A	GRCh38
NC_000006.11:g.51491823G>A , CM000668.1:g.51491823G>A	GRCh37
NC_000006.10:g.51599782G>A	NCBI36
NG_008753.1:g.465601C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.11757C>T MANE Select	ENSP00000360158.3:p.Pro3919=
ENST00000371117.7:c.11757C>T	ENSP00000360158.3:p.Pro3919=
NM_138694.3:c.11757C>T	NP_619639.3:p.Pro3919=
XM_011514679.1:c.11757C>T	XP_011512981.1:p.Pro3919=
XM_011514680.1:c.11757C>T	XP_011512982.1:p.Pro3919=
XM_011514681.1:c.11628C>T	XP_011512983.1:p.Pro3876=
XM_011514682.1:c.11619C>T	XP_011512984.1:p.Pro3873=
XM_011514683.1:c.11115C>T	XP_011512985.1:p.Pro3705=
XM_011514684.1:c.11046C>T	XP_011512986.1:p.Pro3682=
XM_011514690.1:c.5832C>T	XP_011512992.1:p.Pro1944=
XM_011514691.1:c.5832C>T	XP_011512993.1:p.Pro1944=
XM_011514680.3:c.11757C>T	XP_011512982.1:p.Pro3919=
XM_011514682.3:c.11619C>T	XP_011512984.1:p.Pro3873=
XM_011514683.3:c.11115C>T	XP_011512985.1:p.Pro3705=
XM_011514684.3:c.11046C>T	XP_011512986.1:p.Pro3682=
XM_011514690.3:c.5832C>T	XP_011512992.1:p.Pro1944=
XM_011514691.3:c.5832C>T	XP_011512993.1:p.Pro1944=
XM_017010944.2:c.11757C>T	XP_016866433.1:p.Pro3919=
XM_017010945.2:c.11682C>T	XP_016866434.1:p.Pro3894=
XM_017010946.2:c.11562C>T	XP_016866435.1:p.Pro3854=
XM_017010947.2:c.11493C>T	XP_016866436.1:p.Pro3831=
XM_017010948.2:c.11046C>T	XP_016866437.1:p.Pro3682=
XM_017010949.2:c.9897C>T	XP_016866438.1:p.Pro3299=
NM_138694.4:c.11757C>T MANE Select	NP_619639.3:p.Pro3919=