Canonical Allele Identifier: CA1603563405

Gene: RGS14

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177367190G>T , CM000667.2:g.177367190G>T	GRCh38
NC_000005.9:g.176794191G>T , CM000667.1:g.176794191G>T	GRCh37
NC_000005.8:g.176726797G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408923.8:c.483+156G>T MANE Select	ENSP00000386229.3:n.483+156G>T
ENST00000408923.7:c.483+156G>T	ENSP00000386229.3:n.483+156G>T
ENST00000504631.5:n.517+156G>T
ENST00000511890.1:c.92+156G>T
ENST00000514713.5:n.92+156G>T
NM_006480.4:c.483+156G>T	NP_006471.2:n.483+156G>T
XM_005265794.3:c.483+156G>T	XP_005265851.1:n.483+156G>T
XM_005265795.3:c.483+156G>T	XP_005265852.1:n.483+156G>T
NM_001366617.1:c.483+156G>T	NP_001353546.1:n.483+156G>T
NM_001366618.1:c.483+156G>T	NP_001353547.1:n.483+156G>T
XM_024454328.1:c.483+156G>T	XP_024310096.1:n.483+156G>T
NM_006480.5:c.483+156G>T MANE Select	NP_006471.2:n.483+156G>T