Canonical Allele Identifier: CA364438101

Gene: PKHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51775865A>G , CM000668.2:g.51775865A>G	GRCh38
NC_000006.11:g.51640663A>G , CM000668.1:g.51640663A>G	GRCh37
NC_000006.10:g.51748622A>G	NCBI36
NG_008753.1:g.316761T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_138694.4:c.8497T>C MANE Select	NP_619639.3:p.Ser2833Pro
ENST00000371117.8:c.8497T>C MANE Select	ENSP00000360158.3:p.Ser2833Pro
NM_138694.3:c.8497T>C	NP_619639.3:p.Ser2833Pro
NM_170724.2:c.8497T>C	NP_733842.2:p.Ser2833Pro
NM_170724.3:c.8497T>C	NP_733842.2:p.Ser2833Pro
ENST00000340994.4:c.8497T>C	ENSP00000341097.4:p.Ser2833Pro
ENST00000371117.7:c.8497T>C	ENSP00000360158.3:p.Ser2833Pro
XM_011514679.1:c.8497T>C	XP_011512981.1:p.Ser2833Pro
XM_011514680.1:c.8497T>C	XP_011512982.1:p.Ser2833Pro
XM_011514680.3:c.8497T>C	XP_011512982.1:p.Ser2833Pro
XM_011514681.1:c.8368T>C	XP_011512983.1:p.Ser2790Pro
XM_011514682.1:c.8359T>C	XP_011512984.1:p.Ser2787Pro
XM_011514682.3:c.8359T>C	XP_011512984.1:p.Ser2787Pro
XM_011514683.1:c.7855T>C	XP_011512985.1:p.Ser2619Pro
XM_011514683.3:c.7855T>C	XP_011512985.1:p.Ser2619Pro
XM_011514684.1:c.7786T>C	XP_011512986.1:p.Ser2596Pro
XM_011514684.3:c.7786T>C	XP_011512986.1:p.Ser2596Pro
XM_011514685.1:c.8497T>C	XP_011512987.1:p.Ser2833Pro
XM_011514686.1:c.8497T>C	XP_011512988.1:p.Ser2833Pro
XM_011514686.2:c.8497T>C	XP_011512988.1:p.Ser2833Pro
XM_011514687.1:c.8497T>C	XP_011512989.1:p.Ser2833Pro
XM_011514688.1:c.8497T>C	XP_011512990.1:p.Ser2833Pro
XM_011514688.2:c.8497T>C	XP_011512990.1:p.Ser2833Pro
XM_011514690.1:c.2572T>C	XP_011512992.1:p.Ser858Pro
XM_011514690.3:c.2572T>C	XP_011512992.1:p.Ser858Pro
XM_011514691.1:c.2572T>C	XP_011512993.1:p.Ser858Pro
XM_011514691.3:c.2572T>C	XP_011512993.1:p.Ser858Pro
XM_017010944.2:c.8497T>C	XP_016866433.1:p.Ser2833Pro
XM_017010945.2:c.8422T>C	XP_016866434.1:p.Ser2808Pro
XM_017010946.2:c.8302T>C	XP_016866435.1:p.Ser2768Pro
XM_017010947.2:c.8233T>C	XP_016866436.1:p.Ser2745Pro
XM_017010948.2:c.7786T>C	XP_016866437.1:p.Ser2596Pro
XM_017010949.2:c.6637T>C	XP_016866438.1:p.Ser2213Pro
XM_017010950.1:c.8497T>C	XP_016866439.1:p.Ser2833Pro
XM_017010951.1:c.8497T>C	XP_016866440.1:p.Ser2833Pro
XR_001743469.1:n.8773T>C