Canonical Allele Identifier: CA526916178

Gene: RGS4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163070705G>A , CM000663.2:g.163070705G>A	GRCh38
NC_000001.10:g.163040495G>A , CM000663.1:g.163040495G>A	GRCh37
NC_000001.9:g.161307119G>A	NCBI36
NG_023312.1:g.7100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367909.11:c.44+1177G>A MANE Select	ENSP00000356885.6:n.44+1177G>A
ENST00000367908.8:c.44+1177G>A	ENSP00000356884.4:n.44+1177G>A
ENST00000367909.10:c.44+1177G>A	ENSP00000356885.6:n.44+1177G>A
ENST00000421743.6:c.335+1177G>A	ENSP00000397181.2:n.335+1177G>A
ENST00000491263.1:n.166+1177G>A
ENST00000527393.5:n.357+1177G>A
ENST00000527809.5:c.-11+1297G>A	ENSP00000433261.1:n.-11+1297G>A
ENST00000531057.5:c.44+1177G>A	ENSP00000436106.1:n.44+1177G>A
ENST00000533019.1:n.169G>A
NM_001102445.2:c.335+1177G>A	NP_001095915.1:n.335+1177G>A
NM_001113381.1:c.44+1177G>A	NP_001106852.1:n.44+1177G>A
NM_005613.5:c.44+1177G>A	NP_005604.1:n.44+1177G>A
NM_001102445.3:c.335+1177G>A	NP_001095915.1:n.335+1177G>A
NM_005613.6:c.44+1177G>A MANE Select	NP_005604.1:n.44+1177G>A