Canonical Allele Identifier: CA342586938
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153991116-T-A
MyVariant Identifiers: chr1:g.153963592T>A (hg19) chr1:g.153991116T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991116T>A , CM000663.2:g.153991116T>A GRCh38
NC_000001.10:g.153963592T>A , CM000663.1:g.153963592T>A GRCh37
NC_000001.9:g.152230216T>A NCBI36
NG_053102.2:g.5362T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.196T>A
ENST00000643794.1:c.129T>A ENSP00000495765.1:p.Ala43=
ENST00000651669.1:c.8T>A MANE Select ENSP00000499044.1:p.Leu3His
ENST00000368567.4:c.8T>A ENSP00000357555.4:p.Leu3His
ENST00000392558.4:c.8T>A ENSP00000376341.4:p.Leu3His
ENST00000477151.1:n.163T>A
ENST00000493224.5:n.274T>A
NM_001030.4:c.8T>A NP_001021.1:p.Leu3His
NM_001030.6:c.8T>A MANE Select NP_001021.1:p.Leu3His
NM_001349946.1:c.-89T>A NP_001336875.1:n.-89T>A
NM_001349947.1:c.-89T>A NP_001336876.1:n.-89T>A
NM_001349946.2:c.-89T>A NP_001336875.1:n.-89T>A
NM_001349947.2:c.-89T>A NP_001336876.1:n.-89T>A
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