Canonical Allele Identifier: CA364436233

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524588C>A (hg19) ; chr6:g.51659790C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659790C>A , CM000668.2:g.51659790C>A	GRCh38
NC_000006.11:g.51524588C>A , CM000668.1:g.51524588C>A	GRCh37
NC_000006.10:g.51632547C>A	NCBI36
NG_008753.1:g.432836G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10336G>T MANE Select	ENSP00000360158.3:p.Ala3446Ser
ENST00000371117.7:c.10336G>T	ENSP00000360158.3:p.Ala3446Ser
NM_138694.3:c.10336G>T	NP_619639.3:p.Ala3446Ser
XM_011514679.1:c.10336G>T	XP_011512981.1:p.Ala3446Ser
XM_011514680.1:c.10336G>T	XP_011512982.1:p.Ala3446Ser
XM_011514681.1:c.10207G>T	XP_011512983.1:p.Ala3403Ser
XM_011514682.1:c.10198G>T	XP_011512984.1:p.Ala3400Ser
XM_011514683.1:c.9694G>T	XP_011512985.1:p.Ala3232Ser
XM_011514684.1:c.9625G>T	XP_011512986.1:p.Ala3209Ser
XM_011514687.1:c.10157-10570G>T	XP_011512989.1:n.10157-10570G>T
XM_011514690.1:c.4411G>T	XP_011512992.1:p.Ala1471Ser
XM_011514691.1:c.4411G>T	XP_011512993.1:p.Ala1471Ser
XR_926870.1:n.535+7417C>A
XR_926871.1:n.403+7417C>A
XR_926872.1:n.535+7417C>A
XM_011514680.3:c.10336G>T	XP_011512982.1:p.Ala3446Ser
XM_011514682.3:c.10198G>T	XP_011512984.1:p.Ala3400Ser
XM_011514683.3:c.9694G>T	XP_011512985.1:p.Ala3232Ser
XM_011514684.3:c.9625G>T	XP_011512986.1:p.Ala3209Ser
XM_011514690.3:c.4411G>T	XP_011512992.1:p.Ala1471Ser
XM_011514691.3:c.4411G>T	XP_011512993.1:p.Ala1471Ser
XM_017010944.2:c.10336G>T	XP_016866433.1:p.Ala3446Ser
XM_017010945.2:c.10261G>T	XP_016866434.1:p.Ala3421Ser
XM_017010946.2:c.10141G>T	XP_016866435.1:p.Ala3381Ser
XM_017010947.2:c.10072G>T	XP_016866436.1:p.Ala3358Ser
XM_017010948.2:c.9625G>T	XP_016866437.1:p.Ala3209Ser
XM_017010949.2:c.8476G>T	XP_016866438.1:p.Ala2826Ser
XR_001743469.1:n.10612G>T
XR_001744157.1:n.3145+7417C>A
XR_926870.2:n.3145+7417C>A
XR_926871.2:n.3013+7417C>A
XR_926872.2:n.3145+7417C>A
NM_138694.4:c.10336G>T MANE Select	NP_619639.3:p.Ala3446Ser