Canonical Allele Identifier: CA342587643

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991179-T-A
• MyVariant Identifiers: chr1:g.153963655T>A (hg19) ; chr1:g.153991179T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991179T>A , CM000663.2:g.153991179T>A	GRCh38
NC_000001.10:g.153963655T>A , CM000663.1:g.153963655T>A	GRCh37
NC_000001.9:g.152230279T>A	NCBI36
NG_053102.2:g.5425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.259T>A
ENST00000643794.1:c.192T>A	ENSP00000495765.1:p.Pro64=
ENST00000651669.1:c.71T>A MANE Select	ENSP00000499044.1:p.Leu24Gln
ENST00000368567.4:c.71T>A	ENSP00000357555.4:p.Leu24Gln
ENST00000392558.4:c.71T>A	ENSP00000376341.4:p.Leu24Gln
ENST00000477151.1:n.226T>A
ENST00000493224.5:n.337T>A
NM_001030.4:c.71T>A	NP_001021.1:p.Leu24Gln
NM_001030.6:c.71T>A MANE Select	NP_001021.1:p.Leu24Gln
NM_001349946.1:c.-26T>A	NP_001336875.1:n.-26T>A
NM_001349947.1:c.-26T>A	NP_001336876.1:n.-26T>A
NM_001349946.2:c.-26T>A	NP_001336875.1:n.-26T>A
NM_001349947.2:c.-26T>A	NP_001336876.1:n.-26T>A