Canonical Allele Identifier: CA424603415

Gene: RPS7

Linked Data

• MyVariant Identifiers: chr2:g.3623409T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575819T>C , CM000664.2:g.3575819T>C	GRCh38
NC_000002.11:g.3623409T>C , CM000664.1:g.3623409T>C	GRCh37
NC_000002.10:g.3601284T>C	NCBI36
NG_011744.1:g.5557T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.78T>C	ENSP00000385729.3:p.Ala26=
ENST00000491937.6:n.124T>C
ENST00000645674.2:c.78T>C MANE Select	ENSP00000496757.1:p.Ala26=
ENST00000646909.1:c.78T>C	ENSP00000496654.1:p.Ala26=
ENST00000647131.1:c.78T>C	ENSP00000494995.1:p.Ala26=
ENST00000304921.9:c.78T>C	ENSP00000339095.4:p.Ala26=
ENST00000403564.5:c.78T>C	ENSP00000385018.1:p.Ala26=
ENST00000406376.1:c.78T>C	ENSP00000385286.1:p.Ala26=
ENST00000407445.7:c.78T>C	ENSP00000385729.3:p.Ala26=
ENST00000462576.5:n.363T>C
ENST00000479123.1:n.55T>C
ENST00000481006.1:n.330T>C
ENST00000491937.5:n.343T>C
NM_001011.3:c.78T>C	NP_001002.1:p.Ala26=
NM_001011.4:c.78T>C MANE Select	NP_001002.1:p.Ala26=