Canonical Allele Identifier: CA11716807

Gene: DRD5 SLC2A9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9783641G>T , CM000666.2:g.9783641G>T	GRCh38
NC_000004.11:g.9785265G>T , CM000666.1:g.9785265G>T	GRCh37
NC_000004.10:g.9394363G>T	NCBI36
NG_012024.1:g.7008G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304374.4:c.*178G>T (DRD5) MANE Select	ENSP00000306129.2:n.*178G>T
ENST00000304374.3:c.*178G>T (DRD5)	ENSP00000306129.2:n.*178G>T
ENST00000503803.5:n.386-3576C>A (SLC2A9)
ENST00000508585.5:n.182-12272C>A (SLC2A9)
NM_000798.4:c.*178G>T (DRD5)	NP_000789.1:n.*178G>T
XM_006713968.2:c.1601-3576C>A (SLC2A9)	XP_006714031.1:n.1601-3576C>A
XM_011513856.1:c.1420-3576C>A (SLC2A9)	XP_011512158.1:n.1420-3576C>A
XM_011513857.1:c.1333-3576C>A (SLC2A9)	XP_011512159.1:n.1333-3576C>A
XM_011513858.1:c.1333-3576C>A (SLC2A9)	XP_011512160.1:n.1333-3576C>A
XM_011513862.1:c.1024-3576C>A (SLC2A9)	XP_011512164.1:n.1024-3576C>A
XM_011513863.1:c.1024-3576C>A (SLC2A9)	XP_011512165.1:n.1024-3576C>A
XM_011513864.1:c.1012-3576C>A (SLC2A9)	XP_011512166.1:n.1012-3576C>A
XM_011513867.1:c.862-3576C>A (SLC2A9)	XP_011512169.1:n.862-3576C>A
XR_925341.1:n.1697-3576C>A (SLC2A9)
XM_006713968.4:c.1601-3576C>A (SLC2A9)	XP_006714031.1:n.1601-3576C>A
XM_011513856.3:c.1420-3576C>A (SLC2A9)	XP_011512158.1:n.1420-3576C>A
XM_011513862.3:c.1024-3576C>A (SLC2A9)	XP_011512164.1:n.1024-3576C>A
XM_011513864.2:c.1012-3576C>A (SLC2A9)	XP_011512166.1:n.1012-3576C>A
XM_011513867.3:c.862-3576C>A (SLC2A9)	XP_011512169.1:n.862-3576C>A
XM_017008457.2:c.1601-12272C>A (SLC2A9)	XP_016863946.1:n.1601-12272C>A
XM_017008459.1:c.958-3576C>A (SLC2A9)	XP_016863948.1:n.958-3576C>A
XM_024454151.1:c.1033-3576C>A (SLC2A9)	XP_024309919.1:n.1033-3576C>A
XR_925341.3:n.1778-3576C>A (SLC2A9)
NM_000798.5:c.*178G>T (DRD5) MANE Select	NP_000789.1:n.*178G>T