Canonical Allele Identifier: CA364436608

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51524635A>G (hg19) ; chr6:g.51659837A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51659837A>G , CM000668.2:g.51659837A>G	GRCh38
NC_000006.11:g.51524635A>G , CM000668.1:g.51524635A>G	GRCh37
NC_000006.10:g.51632594A>G	NCBI36
NG_008753.1:g.432789T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.10289T>C MANE Select	ENSP00000360158.3:p.Val3430Ala
ENST00000371117.7:c.10289T>C	ENSP00000360158.3:p.Val3430Ala
NM_138694.3:c.10289T>C	NP_619639.3:p.Val3430Ala
XM_011514679.1:c.10289T>C	XP_011512981.1:p.Val3430Ala
XM_011514680.1:c.10289T>C	XP_011512982.1:p.Val3430Ala
XM_011514681.1:c.10160T>C	XP_011512983.1:p.Val3387Ala
XM_011514682.1:c.10151T>C	XP_011512984.1:p.Val3384Ala
XM_011514683.1:c.9647T>C	XP_011512985.1:p.Val3216Ala
XM_011514684.1:c.9578T>C	XP_011512986.1:p.Val3193Ala
XM_011514687.1:c.10157-10617T>C	XP_011512989.1:n.10157-10617T>C
XM_011514690.1:c.4364T>C	XP_011512992.1:p.Val1455Ala
XM_011514691.1:c.4364T>C	XP_011512993.1:p.Val1455Ala
XR_926870.1:n.535+7464A>G
XR_926871.1:n.403+7464A>G
XR_926872.1:n.535+7464A>G
XM_011514680.3:c.10289T>C	XP_011512982.1:p.Val3430Ala
XM_011514682.3:c.10151T>C	XP_011512984.1:p.Val3384Ala
XM_011514683.3:c.9647T>C	XP_011512985.1:p.Val3216Ala
XM_011514684.3:c.9578T>C	XP_011512986.1:p.Val3193Ala
XM_011514690.3:c.4364T>C	XP_011512992.1:p.Val1455Ala
XM_011514691.3:c.4364T>C	XP_011512993.1:p.Val1455Ala
XM_017010944.2:c.10289T>C	XP_016866433.1:p.Val3430Ala
XM_017010945.2:c.10214T>C	XP_016866434.1:p.Val3405Ala
XM_017010946.2:c.10094T>C	XP_016866435.1:p.Val3365Ala
XM_017010947.2:c.10025T>C	XP_016866436.1:p.Val3342Ala
XM_017010948.2:c.9578T>C	XP_016866437.1:p.Val3193Ala
XM_017010949.2:c.8429T>C	XP_016866438.1:p.Val2810Ala
XR_001743469.1:n.10565T>C
XR_001744157.1:n.3145+7464A>G
XR_926870.2:n.3145+7464A>G
XR_926871.2:n.3013+7464A>G
XR_926872.2:n.3145+7464A>G
NM_138694.4:c.10289T>C MANE Select	NP_619639.3:p.Val3430Ala