Canonical Allele Identifier: CA1234620168

Gene: RPS7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575822T= , CM000664.2:g.3575822T=	GRCh38
NC_000002.11:g.3623412T= , CM000664.1:g.3623412T=	GRCh37
NC_000002.10:g.3601287T=	NCBI36
NG_011744.1:g.5560T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.81T=	ENSP00000385729.3:p.Leu27=
ENST00000491937.6:n.127T=
ENST00000645674.2:c.81T= MANE Select	ENSP00000496757.1:p.Leu27=
ENST00000646909.1:c.81T=	ENSP00000496654.1:p.Leu27=
ENST00000647131.1:c.81T=	ENSP00000494995.1:p.Leu27=
ENST00000304921.9:c.81T=	ENSP00000339095.4:p.Leu27=
ENST00000403564.5:c.81T=	ENSP00000385018.1:p.Leu27=
ENST00000406376.1:c.81T=	ENSP00000385286.1:p.Leu27=
ENST00000407445.7:c.81T=	ENSP00000385729.3:p.Leu27=
ENST00000462576.5:n.366T=
ENST00000479123.1:n.58T=
ENST00000481006.1:n.333T=
ENST00000491937.5:n.346T=
NM_001011.3:c.81T=	NP_001002.1:p.Leu27=
NM_001011.4:c.81T= MANE Select	NP_001002.1:p.Leu27=