Canonical Allele Identifier: CA1628626327

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52069414G= , CM000668.2:g.52069414G=	GRCh38
NC_000006.11:g.51934212G= , CM000668.1:g.51934212G=	GRCh37
NC_000006.10:g.52042171G=	NCBI36
NG_008753.1:g.23212C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371117.8:c.778+43C= MANE Select	ENSP00000360158.3:n.778+43C=
ENST00000340994.4:c.778+43C=	ENSP00000341097.4:n.778+43C=
ENST00000371117.7:c.778+43C=	ENSP00000360158.3:n.778+43C=
NM_138694.3:c.778+43C=	NP_619639.3:n.778+43C=
NM_170724.2:c.778+43C=	NP_733842.2:n.778+43C=
XM_011514679.1:c.778+43C=	XP_011512981.1:n.778+43C=
XM_011514680.1:c.778+43C=	XP_011512982.1:n.778+43C=
XM_011514681.1:c.778+43C=	XP_011512983.1:n.778+43C=
XM_011514682.1:c.778+43C=	XP_011512984.1:n.778+43C=
XM_011514683.1:c.778+43C=	XP_011512985.1:n.778+43C=
XM_011514684.1:c.67+43C=	XP_011512986.1:n.67+43C=
XM_011514685.1:c.778+43C=	XP_011512987.1:n.778+43C=
XM_011514686.1:c.778+43C=	XP_011512988.1:n.778+43C=
XM_011514687.1:c.778+43C=	XP_011512989.1:n.778+43C=
XM_011514688.1:c.778+43C=	XP_011512990.1:n.778+43C=
XM_011514689.1:c.778+43C=	XP_011512991.1:n.778+43C=
XR_926869.1:n.389+218G=
XM_011514680.3:c.778+43C=	XP_011512982.1:n.778+43C=
XM_011514682.3:c.778+43C=	XP_011512984.1:n.778+43C=
XM_011514683.3:c.778+43C=	XP_011512985.1:n.778+43C=
XM_011514684.3:c.67+43C=	XP_011512986.1:n.67+43C=
XM_011514686.2:c.778+43C=	XP_011512988.1:n.778+43C=
XM_011514688.2:c.778+43C=	XP_011512990.1:n.778+43C=
XM_017010944.2:c.778+43C=	XP_016866433.1:n.778+43C=
XM_017010945.2:c.703+43C=	XP_016866434.1:n.703+43C=
XM_017010946.2:c.778+43C=	XP_016866435.1:n.778+43C=
XM_017010947.2:c.778+43C=	XP_016866436.1:n.778+43C=
XM_017010948.2:c.67+43C=	XP_016866437.1:n.67+43C=
XM_017010950.1:c.778+43C=	XP_016866439.1:n.778+43C=
XM_017010951.1:c.778+43C=	XP_016866440.1:n.778+43C=
XM_017010952.1:c.778+43C=	XP_016866441.1:n.778+43C=
XR_001743469.1:n.1054+43C=
NM_138694.4:c.778+43C= MANE Select	NP_619639.3:n.778+43C=
NM_170724.3:c.778+43C=	NP_733842.2:n.778+43C=