Canonical Allele Identifier: CA2771053869

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51934399A>G , CM000668.2:g.51934399A>G	GRCh38
NC_000006.11:g.51799197A>G , CM000668.1:g.51799197A>G	GRCh37
NC_000006.10:g.51907156A>G	NCBI36
NG_008753.1:g.158227T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.5909-77T>C MANE Select	ENSP00000360158.3:n.5909-77T>C
ENST00000340994.4:c.5909-77T>C	ENSP00000341097.4:n.5909-77T>C
ENST00000371117.7:c.5909-77T>C	ENSP00000360158.3:n.5909-77T>C
NM_138694.3:c.5909-77T>C	NP_619639.3:n.5909-77T>C
NM_170724.2:c.5909-77T>C	NP_733842.2:n.5909-77T>C
XM_011514679.1:c.5909-77T>C	XP_011512981.1:n.5909-77T>C
XM_011514680.1:c.5909-77T>C	XP_011512982.1:n.5909-77T>C
XM_011514681.1:c.5909-77T>C	XP_011512983.1:n.5909-77T>C
XM_011514682.1:c.5909-77T>C	XP_011512984.1:n.5909-77T>C
XM_011514683.1:c.5267-77T>C	XP_011512985.1:n.5267-77T>C
XM_011514684.1:c.5198-77T>C	XP_011512986.1:n.5198-77T>C
XM_011514685.1:c.5909-77T>C	XP_011512987.1:n.5909-77T>C
XM_011514686.1:c.5909-77T>C	XP_011512988.1:n.5909-77T>C
XM_011514687.1:c.5909-77T>C	XP_011512989.1:n.5909-77T>C
XM_011514688.1:c.5909-77T>C	XP_011512990.1:n.5909-77T>C
XM_011514689.1:c.5909-77T>C	XP_011512991.1:n.5909-77T>C
XM_011514690.1:c.-17-77T>C	XP_011512992.1:n.-17-77T>C
XM_011514691.1:c.-17-77T>C	XP_011512993.1:n.-17-77T>C
XM_011514680.3:c.5909-77T>C	XP_011512982.1:n.5909-77T>C
XM_011514682.3:c.5909-77T>C	XP_011512984.1:n.5909-77T>C
XM_011514683.3:c.5267-77T>C	XP_011512985.1:n.5267-77T>C
XM_011514684.3:c.5198-77T>C	XP_011512986.1:n.5198-77T>C
XM_011514686.2:c.5909-77T>C	XP_011512988.1:n.5909-77T>C
XM_011514688.2:c.5909-77T>C	XP_011512990.1:n.5909-77T>C
XM_011514690.3:c.-17-77T>C	XP_011512992.1:n.-17-77T>C
XM_011514691.3:c.-17-77T>C	XP_011512993.1:n.-17-77T>C
XM_017010944.2:c.5909-77T>C	XP_016866433.1:n.5909-77T>C
XM_017010945.2:c.5834-77T>C	XP_016866434.1:n.5834-77T>C
XM_017010946.2:c.5909-77T>C	XP_016866435.1:n.5909-77T>C
XM_017010947.2:c.5645-77T>C	XP_016866436.1:n.5645-77T>C
XM_017010948.2:c.5198-77T>C	XP_016866437.1:n.5198-77T>C
XM_017010949.2:c.4049-77T>C	XP_016866438.1:n.4049-77T>C
XM_017010950.1:c.5909-77T>C	XP_016866439.1:n.5909-77T>C
XM_017010951.1:c.5909-77T>C	XP_016866440.1:n.5909-77T>C
XM_017010952.1:c.5909-77T>C	XP_016866441.1:n.5909-77T>C
XR_001743469.1:n.6185-77T>C
NM_138694.4:c.5909-77T>C MANE Select	NP_619639.3:n.5909-77T>C
NM_170724.3:c.5909-77T>C	NP_733842.2:n.5909-77T>C