Canonical Allele Identifier: CA15388292

Gene: RPS14

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150446307C>T , CM000667.2:g.150446307C>T	GRCh38
NC_000005.9:g.149825870C>T , CM000667.1:g.149825870C>T	GRCh37
NC_000005.8:g.149806063C>T	NCBI36
NG_042287.1:g.8450G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312037.6:c.311+495G>A	ENSP00000311028.5:n.311+495G>A
ENST00000401695.8:c.311+495G>A	ENSP00000385958.3:n.311+495G>A
ENST00000407193.7:c.311+495G>A MANE Select	ENSP00000385425.1:n.311+495G>A
ENST00000642507.1:c.311+495G>A	ENSP00000496665.1:n.311+495G>A
ENST00000312037.5:c.311+495G>A	ENSP00000311028.5:n.311+495G>A
ENST00000401695.7:c.311+495G>A	ENSP00000385958.3:n.311+495G>A
ENST00000407193.5:c.311+495G>A	ENSP00000385425.1:n.311+495G>A
ENST00000518139.5:c.311+495G>A	ENSP00000429856.1:n.311+495G>A
ENST00000519690.1:n.2926+495G>A
ENST00000519855.1:c.136+495G>A
ENST00000521466.5:c.311+495G>A	ENSP00000428509.1:n.311+495G>A
NM_001025070.1:c.311+495G>A	NP_001020241.1:n.311+495G>A
NM_001025071.1:c.311+495G>A	NP_001020242.1:n.311+495G>A
NM_005617.3:c.311+495G>A	NP_005608.1:n.311+495G>A
NM_005617.4:c.311+495G>A MANE Select	NP_005608.1:n.311+495G>A
NM_001025070.2:c.311+495G>A	NP_001020241.1:n.311+495G>A
NM_001025071.2:c.311+495G>A	NP_001020242.1:n.311+495G>A