Canonical Allele Identifier: CA2822462

Gene: GRK4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.2988772G>A , CM000666.2:g.2988772G>A	GRCh38
NC_000004.11:g.2990499G>A , CM000666.1:g.2990499G>A	GRCh37
NC_000004.10:g.2960297G>A	NCBI36
NG_029102.1:g.30157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398052.9:c.194G>A MANE Select	ENSP00000381129.4:p.Arg65His
ENST00000345167.10:c.98G>A	ENSP00000264764.8:p.Arg33His
ENST00000398051.8:c.98G>A	ENSP00000381128.4:p.Arg33His
ENST00000398052.8:c.194G>A	ENSP00000381129.4:p.Arg65His
ENST00000504933.1:c.194G>A	ENSP00000427445.1:p.Arg65His
NM_001004056.1:c.98G>A	NP_001004056.1:p.Arg33His
NM_001004057.1:c.194G>A	NP_001004057.1:p.Arg65His
NM_005307.2:c.98G>A	NP_005298.2:p.Arg33His
NM_182982.2:c.194G>A	NP_892027.2:p.Arg65His
XM_005247962.2:c.-372-3443G>A	XP_005248019.1:n.-372-3443G>A
XM_006713880.2:c.-400-3443G>A	XP_006713943.1:n.-400-3443G>A
XM_011513447.1:c.194G>A	XP_011511749.1:p.Arg65His
XM_011513448.1:c.194G>A	XP_011511750.1:p.Arg65His
XM_011513449.1:c.98G>A	XP_011511751.1:p.Arg33His
XM_011513450.1:c.194G>A	XP_011511752.1:p.Arg65His
XM_011513451.1:c.194G>A	XP_011511753.1:p.Arg65His
XM_011513452.1:c.194G>A	XP_011511754.1:p.Arg65His
XM_011513453.1:c.194G>A	XP_011511755.1:p.Arg65His
XM_011513454.1:c.194G>A	XP_011511756.1:p.Arg65His
XM_011513455.1:c.194G>A	XP_011511757.1:p.Arg65His
XM_011513456.1:c.194G>A	XP_011511758.1:p.Arg65His
XM_011513457.1:c.194G>A	XP_011511759.1:p.Arg65His
XR_924941.1:n.760G>A
XR_924943.1:n.760G>A
NM_001350173.1:c.-285-3443G>A	NP_001337102.1:n.-285-3443G>A
XM_005247962.3:c.-372-3443G>A	XP_005248019.1:n.-372-3443G>A
XM_006713880.3:c.-400-3443G>A	XP_006713943.1:n.-400-3443G>A
XM_011513447.2:c.194G>A	XP_011511749.1:p.Arg65His
XM_011513448.2:c.194G>A	XP_011511750.1:p.Arg65His
XM_011513449.2:c.98G>A	XP_011511751.1:p.Arg33His
XM_011513450.2:c.194G>A	XP_011511752.1:p.Arg65His
XM_011513451.2:c.194G>A	XP_011511753.1:p.Arg65His
XM_011513452.2:c.194G>A	XP_011511754.1:p.Arg65His
XM_011513453.2:c.194G>A	XP_011511755.1:p.Arg65His
XM_011513454.2:c.194G>A	XP_011511756.1:p.Arg65His
XM_011513455.2:c.194G>A	XP_011511757.1:p.Arg65His
XM_011513456.2:c.194G>A	XP_011511758.1:p.Arg65His
XM_011513457.2:c.194G>A	XP_011511759.1:p.Arg65His
XM_017008052.1:c.194G>A	XP_016863541.1:p.Arg65His
XM_017008053.1:c.194G>A	XP_016863542.1:p.Arg65His
XM_017008054.1:c.194G>A	XP_016863543.1:p.Arg65His
XM_017008055.1:c.98G>A	XP_016863544.1:p.Arg33His
XM_017008056.1:c.194G>A	XP_016863545.1:p.Arg65His
XM_017008057.1:c.-257-3443G>A	XP_016863546.1:n.-257-3443G>A
XM_017008058.1:c.-309-3443G>A	XP_016863547.1:n.-309-3443G>A
XM_017008059.2:c.-257-3443G>A	XP_016863548.1:n.-257-3443G>A
XM_017008062.1:c.-372-3443G>A	XP_016863551.1:n.-372-3443G>A
XM_017008063.1:c.-325G>A	XP_016863552.1:n.-325G>A
XM_017008064.1:c.-325G>A	XP_016863553.1:n.-325G>A
XM_017008065.1:c.194G>A	XP_016863554.1:p.Arg65His
XM_017008066.1:c.-257-3443G>A	XP_016863555.1:n.-257-3443G>A
XM_024454015.1:c.-325G>A	XP_024309783.1:n.-325G>A
XR_001741210.1:n.761G>A
XR_001741211.1:n.761G>A
XR_924941.2:n.761G>A
XR_924943.2:n.761G>A
NM_182982.3:c.194G>A MANE Select	NP_892027.2:p.Arg65His
NM_001004056.2:c.98G>A	NP_001004056.1:p.Arg33His
NM_001004057.2:c.194G>A	NP_001004057.1:p.Arg65His
NM_001350173.2:c.-285-3443G>A	NP_001337102.1:n.-285-3443G>A
NM_005307.3:c.98G>A	NP_005298.2:p.Arg33His