Canonical Allele Identifier: CA345742677

Gene: RPS7

Linked Data

• MyVariant Identifiers: chr2:g.3623406G>C (hg19) ; chr2:g.3575816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575816G>C , CM000664.2:g.3575816G>C	GRCh38
NC_000002.11:g.3623406G>C , CM000664.1:g.3623406G>C	GRCh37
NC_000002.10:g.3601281G>C	NCBI36
NG_011744.1:g.5554G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.76-1G>C	ENSP00000385729.3:n.76-1G>C
ENST00000491937.6:n.122-1G>C
ENST00000645674.2:c.76-1G>C MANE Select	ENSP00000496757.1:n.76-1G>C
ENST00000646909.1:c.76-1G>C	ENSP00000496654.1:n.76-1G>C
ENST00000647131.1:c.76-1G>C	ENSP00000494995.1:n.76-1G>C
ENST00000304921.9:c.76-1G>C	ENSP00000339095.4:n.76-1G>C
ENST00000403564.5:c.76-1G>C	ENSP00000385018.1:n.76-1G>C
ENST00000406376.1:c.76-1G>C	ENSP00000385286.1:n.76-1G>C
ENST00000407445.7:c.76-1G>C	ENSP00000385729.3:n.76-1G>C
ENST00000462576.5:n.361-1G>C
ENST00000479123.1:n.53-1G>C
ENST00000481006.1:n.328-1G>C
ENST00000491937.5:n.341-1G>C
NM_001011.3:c.76-1G>C	NP_001002.1:n.76-1G>C
NM_001011.4:c.76-1G>C MANE Select	NP_001002.1:n.76-1G>C