Canonical Allele Identifier: CA1139949725

Gene: RGS4

Genomic Alleles

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

Transcript Alleles

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