Canonical Allele Identifier: CA345742698

Gene: RPS7

Linked Data

• MyVariant Identifiers: chr2:g.3623417A>T (hg19) ; chr2:g.3575827A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575827A>T , CM000664.2:g.3575827A>T	GRCh38
NC_000002.11:g.3623417A>T , CM000664.1:g.3623417A>T	GRCh37
NC_000002.10:g.3601292A>T	NCBI36
NG_011744.1:g.5565A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.86A>T	ENSP00000385729.3:p.Glu29Val
ENST00000491937.6:n.132A>T
ENST00000645674.2:c.86A>T MANE Select	ENSP00000496757.1:p.Glu29Val
ENST00000646909.1:c.86A>T	ENSP00000496654.1:p.Glu29Val
ENST00000647131.1:c.86A>T	ENSP00000494995.1:p.Glu29Val
ENST00000304921.9:c.86A>T	ENSP00000339095.4:p.Glu29Val
ENST00000403564.5:c.86A>T	ENSP00000385018.1:p.Glu29Val
ENST00000406376.1:c.86A>T	ENSP00000385286.1:p.Glu29Val
ENST00000407445.7:c.86A>T	ENSP00000385729.3:p.Glu29Val
ENST00000462576.5:n.371A>T
ENST00000479123.1:n.63A>T
ENST00000481006.1:n.338A>T
ENST00000491937.5:n.351A>T
NM_001011.3:c.86A>T	NP_001002.1:p.Glu29Val
NM_001011.4:c.86A>T MANE Select	NP_001002.1:p.Glu29Val