Canonical Allele Identifier: CA3217640348

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2118760G= , CM000678.2:g.2118760G=	GRCh38
NC_000016.9:g.2168761G= , CM000678.1:g.2168761G=	GRCh37
NC_000016.8:g.2108762G=	NCBI36
NG_008617.1:g.22139C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001009944.3:c.445C= MANE Select	NP_001009944.3:p.Gln149=
ENST00000262304.9:c.445C= MANE Select	ENSP00000262304.4:p.Gln149=
NM_000296.3:c.445C=	NP_000287.3:p.Gln149=
NM_000296.4:c.445C=	NP_000287.4:p.Gln149=
NM_001009944.2:c.445C=	NP_001009944.2:p.Gln149=
ENST00000262304.8:c.445C=	ENSP00000262304.4:p.Gln149=
ENST00000423118.5:c.445C=	ENSP00000399501.1:p.Gln149=
XM_011522525.1:c.499C=	XP_011520827.1:p.Gln167=
XM_011522526.1:c.499C=	XP_011520828.1:p.Gln167=
XM_011522527.1:c.499C=	XP_011520829.1:p.Gln167=
XM_011522528.1:c.499C=	XP_011520830.1:p.Gln167=
XM_011522528.3:c.499C=	XP_011520830.1:p.Gln167=
XM_011522529.1:c.499C=	XP_011520831.1:p.Gln167=
XM_011522529.2:c.499C=	XP_011520831.1:p.Gln167=
XM_011522530.1:c.445C=	XP_011520832.1:p.Gln149=
XM_011522531.1:c.427C=	XP_011520833.1:p.Gln143=
XM_011522532.1:c.373C=	XP_011520834.1:p.Gln125=
XM_011522533.1:c.292C=	XP_011520835.1:p.Gln98=
XM_011522534.1:c.235C=	XP_011520836.1:p.Gln79=
XM_011522536.1:c.499C=	XP_011520838.1:p.Gln167=
XM_024450298.1:c.445C=	XP_024306066.1:p.Gln149=
XM_024450299.1:c.373C=	XP_024306067.1:p.Gln125=
XM_024450300.1:c.235C=	XP_024306068.1:p.Gln79=
XR_932867.1:n.514C=
XR_932868.1:n.514C=
XR_932869.1:n.514C=
XR_932870.1:n.514C=