Canonical Allele Identifier: CA2580584411

Gene: RGS4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163069987T>A , CM000663.2:g.163069987T>A	GRCh38
NC_000001.10:g.163039777T>A , CM000663.1:g.163039777T>A	GRCh37
NC_000001.9:g.161306401T>A	NCBI36
NG_023312.1:g.6382T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367909.11:c.44+459T>A MANE Select	ENSP00000356885.6:n.44+459T>A
ENST00000367908.8:c.44+459T>A	ENSP00000356884.4:n.44+459T>A
ENST00000367909.10:c.44+459T>A	ENSP00000356885.6:n.44+459T>A
ENST00000421743.6:c.335+459T>A	ENSP00000397181.2:n.335+459T>A
ENST00000491263.1:n.166+459T>A
ENST00000527393.5:n.357+459T>A
ENST00000527809.5:c.-11+579T>A	ENSP00000433261.1:n.-11+579T>A
ENST00000531057.5:c.44+459T>A	ENSP00000436106.1:n.44+459T>A
NM_001102445.2:c.335+459T>A	NP_001095915.1:n.335+459T>A
NM_001113381.1:c.44+459T>A	NP_001106852.1:n.44+459T>A
NM_005613.5:c.44+459T>A	NP_005604.1:n.44+459T>A
NM_001102445.3:c.335+459T>A	NP_001095915.1:n.335+459T>A
NM_005613.6:c.44+459T>A MANE Select	NP_005604.1:n.44+459T>A