Canonical Allele Identifier: CA1139929878

Gene: RGS4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.163071074G= , CM000663.2:g.163071074G=	GRCh38
NC_000001.10:g.163040864G= , CM000663.1:g.163040864G=	GRCh37
NC_000001.9:g.161307488G=	NCBI36
NG_023312.1:g.7469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367909.11:c.45-1321G= MANE Select	ENSP00000356885.6:n.45-1321G=
ENST00000367908.8:c.45-1321G=	ENSP00000356884.4:n.45-1321G=
ENST00000367909.10:c.45-1321G=	ENSP00000356885.6:n.45-1321G=
ENST00000421743.6:c.336-1321G=	ENSP00000397181.2:n.336-1321G=
ENST00000491263.1:n.167-1321G=
ENST00000527393.5:n.358-1321G=
ENST00000527809.5:c.-10-1321G=	ENSP00000433261.1:n.-10-1321G=
ENST00000531057.5:c.45-1321G=	ENSP00000436106.1:n.45-1321G=
ENST00000533019.1:n.183+355G=
NM_001102445.2:c.336-1321G=	NP_001095915.1:n.336-1321G=
NM_001113381.1:c.45-1321G=	NP_001106852.1:n.45-1321G=
NM_005613.5:c.45-1321G=	NP_005604.1:n.45-1321G=
NM_001102445.3:c.336-1321G=	NP_001095915.1:n.336-1321G=
NM_005613.6:c.45-1321G= MANE Select	NP_005604.1:n.45-1321G=