Canonical Allele Identifier: CA364421022

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51612957A>C (hg19) ; chr6:g.51748159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51748159A>C , CM000668.2:g.51748159A>C	GRCh38
NC_000006.11:g.51612957A>C , CM000668.1:g.51612957A>C	GRCh37
NC_000006.10:g.51720916A>C	NCBI36
NG_008753.1:g.344467T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.9457T>G MANE Select	ENSP00000360158.3:p.Phe3153Val
ENST00000340994.4:c.9457T>G	ENSP00000341097.4:p.Phe3153Val
ENST00000371117.7:c.9457T>G	ENSP00000360158.3:p.Phe3153Val
NM_138694.3:c.9457T>G	NP_619639.3:p.Phe3153Val
NM_170724.2:c.9457T>G	NP_733842.2:p.Phe3153Val
XM_011514679.1:c.9457T>G	XP_011512981.1:p.Phe3153Val
XM_011514680.1:c.9457T>G	XP_011512982.1:p.Phe3153Val
XM_011514681.1:c.9328T>G	XP_011512983.1:p.Phe3110Val
XM_011514682.1:c.9319T>G	XP_011512984.1:p.Phe3107Val
XM_011514683.1:c.8815T>G	XP_011512985.1:p.Phe2939Val
XM_011514684.1:c.8746T>G	XP_011512986.1:p.Phe2916Val
XM_011514685.1:c.9457T>G	XP_011512987.1:p.Phe3153Val
XM_011514686.1:c.9457T>G	XP_011512988.1:p.Phe3153Val
XM_011514687.1:c.9457T>G	XP_011512989.1:p.Phe3153Val
XM_011514688.1:c.9457T>G	XP_011512990.1:p.Phe3153Val
XM_011514690.1:c.3532T>G	XP_011512992.1:p.Phe1178Val
XM_011514691.1:c.3532T>G	XP_011512993.1:p.Phe1178Val
XM_011514680.3:c.9457T>G	XP_011512982.1:p.Phe3153Val
XM_011514682.3:c.9319T>G	XP_011512984.1:p.Phe3107Val
XM_011514683.3:c.8815T>G	XP_011512985.1:p.Phe2939Val
XM_011514684.3:c.8746T>G	XP_011512986.1:p.Phe2916Val
XM_011514686.2:c.9457T>G	XP_011512988.1:p.Phe3153Val
XM_011514688.2:c.9457T>G	XP_011512990.1:p.Phe3153Val
XM_011514690.3:c.3532T>G	XP_011512992.1:p.Phe1178Val
XM_011514691.3:c.3532T>G	XP_011512993.1:p.Phe1178Val
XM_017010944.2:c.9457T>G	XP_016866433.1:p.Phe3153Val
XM_017010945.2:c.9382T>G	XP_016866434.1:p.Phe3128Val
XM_017010946.2:c.9262T>G	XP_016866435.1:p.Phe3088Val
XM_017010947.2:c.9193T>G	XP_016866436.1:p.Phe3065Val
XM_017010948.2:c.8746T>G	XP_016866437.1:p.Phe2916Val
XM_017010949.2:c.7597T>G	XP_016866438.1:p.Phe2533Val
XM_017010950.1:c.9457T>G	XP_016866439.1:p.Phe3153Val
XR_001743469.1:n.9733T>G
NM_138694.4:c.9457T>G MANE Select	NP_619639.3:p.Phe3153Val
NM_170724.3:c.9457T>G	NP_733842.2:p.Phe3153Val