Canonical Allele Identifier: CA1234620165

Gene: RPS7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575818C= , CM000664.2:g.3575818C=	GRCh38
NC_000002.11:g.3623408C= , CM000664.1:g.3623408C=	GRCh37
NC_000002.10:g.3601283C=	NCBI36
NG_011744.1:g.5556C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.77C=	ENSP00000385729.3:p.Ala26=
ENST00000491937.6:n.123C=
ENST00000645674.2:c.77C= MANE Select	ENSP00000496757.1:p.Ala26=
ENST00000646909.1:c.77C=	ENSP00000496654.1:p.Ala26=
ENST00000647131.1:c.77C=	ENSP00000494995.1:p.Ala26=
ENST00000304921.9:c.77C=	ENSP00000339095.4:p.Ala26=
ENST00000403564.5:c.77C=	ENSP00000385018.1:p.Ala26=
ENST00000406376.1:c.77C=	ENSP00000385286.1:p.Ala26=
ENST00000407445.7:c.77C=	ENSP00000385729.3:p.Ala26=
ENST00000462576.5:n.362C=
ENST00000479123.1:n.54C=
ENST00000481006.1:n.329C=
ENST00000491937.5:n.342C=
NM_001011.3:c.77C=	NP_001002.1:p.Ala26=
NM_001011.4:c.77C= MANE Select	NP_001002.1:p.Ala26=