Canonical Allele Identifier: CA424603420

Gene: RPS7

Linked Data

• MyVariant Identifiers: chr2:g.3623415G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575825G>T , CM000664.2:g.3575825G>T	GRCh38
NC_000002.11:g.3623415G>T , CM000664.1:g.3623415G>T	GRCh37
NC_000002.10:g.3601290G>T	NCBI36
NG_011744.1:g.5563G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.84G>T	ENSP00000385729.3:p.Leu28=
ENST00000491937.6:n.130G>T
ENST00000645674.2:c.84G>T MANE Select	ENSP00000496757.1:p.Leu28=
ENST00000646909.1:c.84G>T	ENSP00000496654.1:p.Leu28=
ENST00000647131.1:c.84G>T	ENSP00000494995.1:p.Leu28=
ENST00000304921.9:c.84G>T	ENSP00000339095.4:p.Leu28=
ENST00000403564.5:c.84G>T	ENSP00000385018.1:p.Leu28=
ENST00000406376.1:c.84G>T	ENSP00000385286.1:p.Leu28=
ENST00000407445.7:c.84G>T	ENSP00000385729.3:p.Leu28=
ENST00000462576.5:n.369G>T
ENST00000479123.1:n.61G>T
ENST00000481006.1:n.336G>T
ENST00000491937.5:n.349G>T
NM_001011.3:c.84G>T	NP_001002.1:p.Leu28=
NM_001011.4:c.84G>T MANE Select	NP_001002.1:p.Leu28=