Canonical Allele Identifier: CA1603571672

Gene: RGS14

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177371305G>C , CM000667.2:g.177371305G>C	GRCh38
NC_000005.9:g.176798306G>C , CM000667.1:g.176798306G>C	GRCh37
NC_000005.8:g.176730912G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000408923.8:c.1337-45G>C MANE Select	ENSP00000386229.3:n.1337-45G>C
ENST00000408923.7:c.1337-45G>C	ENSP00000386229.3:n.1337-45G>C
ENST00000425155.6:n.1444-45G>C
ENST00000502731.5:n.322-45G>C
ENST00000503044.5:n.141-45G>C
ENST00000506944.1:n.135-45G>C
ENST00000509289.1:n.182-45G>C
ENST00000511890.1:c.949-45G>C
ENST00000514102.5:n.294-45G>C
NM_006480.4:c.1337-45G>C	NP_006471.2:n.1337-45G>C
XM_005265794.3:c.1340-45G>C	XP_005265851.1:n.1340-45G>C
XM_005265795.3:c.1340-45G>C	XP_005265852.1:n.1340-45G>C
NM_001366617.1:c.1340-45G>C	NP_001353546.1:n.1340-45G>C
NM_001366618.1:c.1340-45G>C	NP_001353547.1:n.1340-45G>C
XM_024454328.1:c.1340-45G>C	XP_024310096.1:n.1340-45G>C
NM_006480.5:c.1337-45G>C MANE Select	NP_006471.2:n.1337-45G>C