Canonical Allele Identifier: CA1603568729

Gene: RGS14

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177370342G= , CM000667.2:g.177370342G=	GRCh38
NC_000005.9:g.176797343G= , CM000667.1:g.176797343G=	GRCh37
NC_000005.8:g.176729949G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006480.5:c.1054-249G= MANE Select	NP_006471.2:n.1054-249G=
ENST00000408923.8:c.1054-249G= MANE Select	ENSP00000386229.3:n.1054-249G=
NM_001366617.1:c.1054-246G=	NP_001353546.1:n.1054-246G=
NM_001366618.1:c.1054-246G=	NP_001353547.1:n.1054-246G=
NM_006480.4:c.1054-249G=	NP_006471.2:n.1054-249G=
ENST00000408923.7:c.1054-249G=	ENSP00000386229.3:n.1054-249G=
ENST00000425155.6:n.1158-246G=
ENST00000511890.1:c.663-246G=
XM_005265794.3:c.1054-246G=	XP_005265851.1:n.1054-246G=
XM_005265795.3:c.1054-246G=	XP_005265852.1:n.1054-246G=
XM_024454328.1:c.1054-246G=	XP_024310096.1:n.1054-246G=