Canonical Allele Identifier: CA364436920

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524669C>A (hg19) ; chr6:g.51659871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659871C>A , CM000668.2:g.51659871C>A	GRCh38
NC_000006.11:g.51524669C>A , CM000668.1:g.51524669C>A	GRCh37
NC_000006.10:g.51632628C>A	NCBI36
NG_008753.1:g.432755G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10255G>T MANE Select	ENSP00000360158.3:p.Asp3419Tyr
ENST00000371117.7:c.10255G>T	ENSP00000360158.3:p.Asp3419Tyr
NM_138694.3:c.10255G>T	NP_619639.3:p.Asp3419Tyr
XM_011514679.1:c.10255G>T	XP_011512981.1:p.Asp3419Tyr
XM_011514680.1:c.10255G>T	XP_011512982.1:p.Asp3419Tyr
XM_011514681.1:c.10126G>T	XP_011512983.1:p.Asp3376Tyr
XM_011514682.1:c.10117G>T	XP_011512984.1:p.Asp3373Tyr
XM_011514683.1:c.9613G>T	XP_011512985.1:p.Asp3205Tyr
XM_011514684.1:c.9544G>T	XP_011512986.1:p.Asp3182Tyr
XM_011514687.1:c.10157-10651G>T	XP_011512989.1:n.10157-10651G>T
XM_011514690.1:c.4330G>T	XP_011512992.1:p.Asp1444Tyr
XM_011514691.1:c.4330G>T	XP_011512993.1:p.Asp1444Tyr
XR_926870.1:n.535+7498C>A
XR_926871.1:n.403+7498C>A
XR_926872.1:n.535+7498C>A
XM_011514680.3:c.10255G>T	XP_011512982.1:p.Asp3419Tyr
XM_011514682.3:c.10117G>T	XP_011512984.1:p.Asp3373Tyr
XM_011514683.3:c.9613G>T	XP_011512985.1:p.Asp3205Tyr
XM_011514684.3:c.9544G>T	XP_011512986.1:p.Asp3182Tyr
XM_011514690.3:c.4330G>T	XP_011512992.1:p.Asp1444Tyr
XM_011514691.3:c.4330G>T	XP_011512993.1:p.Asp1444Tyr
XM_017010944.2:c.10255G>T	XP_016866433.1:p.Asp3419Tyr
XM_017010945.2:c.10180G>T	XP_016866434.1:p.Asp3394Tyr
XM_017010946.2:c.10060G>T	XP_016866435.1:p.Asp3354Tyr
XM_017010947.2:c.9991G>T	XP_016866436.1:p.Asp3331Tyr
XM_017010948.2:c.9544G>T	XP_016866437.1:p.Asp3182Tyr
XM_017010949.2:c.8395G>T	XP_016866438.1:p.Asp2799Tyr
XR_001743469.1:n.10531G>T
XR_001744157.1:n.3145+7498C>A
XR_926870.2:n.3145+7498C>A
XR_926871.2:n.3013+7498C>A
XR_926872.2:n.3145+7498C>A
NM_138694.4:c.10255G>T MANE Select	NP_619639.3:p.Asp3419Tyr