Canonical Allele Identifier: CA31819120

Gene: RGS4

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163076561G>A , CM000663.2:g.163076561G>A	GRCh38
NC_000001.10:g.163046351G>A , CM000663.1:g.163046351G>A	GRCh37
NC_000001.9:g.161312975G>A	NCBI36
NG_023312.1:g.12956G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367909.11:c.*2001G>A MANE Select	ENSP00000356885.6:n.*2001G>A
ENST00000367908.8:c.*2170G>A	ENSP00000356884.4:n.*2170G>A
ENST00000367909.10:c.*2001G>A	ENSP00000356885.6:n.*2001G>A
ENST00000421743.6:c.*2001G>A	ENSP00000397181.2:n.*2001G>A
ENST00000491263.1:n.3744G>A
NM_001102445.2:c.*2001G>A	NP_001095915.1:n.*2001G>A
NM_001113380.1:c.*2001G>A	NP_001106851.1:n.*2001G>A
NM_001113381.1:c.*2170G>A	NP_001106852.1:n.*2170G>A
NM_005613.5:c.*2001G>A	NP_005604.1:n.*2001G>A
NM_001102445.3:c.*2001G>A	NP_001095915.1:n.*2001G>A
NM_005613.6:c.*2001G>A MANE Select	NP_005604.1:n.*2001G>A