Canonical Allele Identifier: CA41546167

Gene: RPS7

Linked Data

• dbSNP Id: rs142474961
• MyVariant Identifiers: chr2:g.3623407G>A (hg19) ; chr2:g.3575817G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3575817G>A , CM000664.2:g.3575817G>A	GRCh38
NC_000002.11:g.3623407G>A , CM000664.1:g.3623407G>A	GRCh37
NC_000002.10:g.3601282G>A	NCBI36
NG_011744.1:g.5555G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000407445.8:c.76G>A	ENSP00000385729.3:p.Ala26Thr
ENST00000491937.6:n.122G>A
ENST00000645674.2:c.76G>A MANE Select	ENSP00000496757.1:p.Ala26Thr
ENST00000646909.1:c.76G>A	ENSP00000496654.1:p.Ala26Thr
ENST00000647131.1:c.76G>A	ENSP00000494995.1:p.Ala26Thr
ENST00000304921.9:c.76G>A	ENSP00000339095.4:p.Ala26Thr
ENST00000403564.5:c.76G>A	ENSP00000385018.1:p.Ala26Thr
ENST00000406376.1:c.76G>A	ENSP00000385286.1:p.Ala26Thr
ENST00000407445.7:c.76G>A	ENSP00000385729.3:p.Ala26Thr
ENST00000462576.5:n.361G>A
ENST00000479123.1:n.53G>A
ENST00000481006.1:n.328G>A
ENST00000491937.5:n.341G>A
NM_001011.3:c.76G>A	NP_001002.1:p.Ala26Thr
NM_001011.4:c.76G>A MANE Select	NP_001002.1:p.Ala26Thr