Canonical Allele Identifier: CA1139773648

Gene: RGS4

Genomic Alleles

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

Transcript Alleles

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