Canonical Allele Identifier: CA9973630

Gene: RGS19

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.64076582G>A , CM000682.2:g.64076582G>A	GRCh38
NC_000020.10:g.62707935G>A , CM000682.1:g.62707935G>A	GRCh37
NC_000020.9:g.62178379G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395042.2:c.95C>T MANE Select	ENSP00000378483.1:p.Ala32Val
ENST00000332298.9:c.95C>T	ENSP00000333194.5:p.Ala32Val
ENST00000395042.1:c.95C>T	ENSP00000378483.1:p.Ala32Val
ENST00000479996.1:n.197C>T
ENST00000493165.1:n.681C>T
NM_001039467.1:c.95C>T	NP_001034556.1:p.Ala32Val
NM_005873.2:c.95C>T	NP_005864.1:p.Ala32Val
XM_005260182.2:c.29C>T	XP_005260239.1:p.Ala10Val
XM_005260183.1:c.29C>T	XP_005260240.1:p.Ala10Val
XM_011528484.1:c.182C>T	XP_011526786.1:p.Ala61Val
XM_011528485.1:c.95C>T	XP_011526787.1:p.Ala32Val
XM_011528486.1:c.95C>T	XP_011526788.1:p.Ala32Val
XM_005260182.3:c.29C>T	XP_005260239.1:p.Ala10Val
XM_005260183.2:c.29C>T	XP_005260240.1:p.Ala10Val
XM_011528484.2:c.182C>T	XP_011526786.1:p.Ala61Val
XM_011528485.2:c.95C>T	XP_011526787.1:p.Ala32Val
XM_011528486.2:c.95C>T	XP_011526788.1:p.Ala32Val
NM_005873.3:c.95C>T MANE Select	NP_005864.1:p.Ala32Val
NM_001039467.2:c.95C>T	NP_001034556.1:p.Ala32Val