Canonical Allele Identifier: CA2573911218

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990891C>A , CM000663.2:g.153990891C>A	GRCh38
NC_000001.10:g.153963367C>A , CM000663.1:g.153963367C>A	GRCh37
NC_000001.9:g.152229991C>A	NCBI36
NG_053102.2:g.5137C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.7-23C>A	ENSP00000495765.1:n.7-23C>A
ENST00000651669.1:c.6+89C>A MANE Select	ENSP00000499044.1:n.6+89C>A
ENST00000368567.4:c.6+89C>A	ENSP00000357555.4:n.6+89C>A
ENST00000392558.4:c.6+89C>A	ENSP00000376341.4:n.6+89C>A
ENST00000477151.1:n.41-23C>A
ENST00000493224.5:n.129C>A
NM_001030.4:c.6+89C>A	NP_001021.1:n.6+89C>A
NM_001030.6:c.6+89C>A MANE Select	NP_001021.1:n.6+89C>A
NM_001349946.1:c.-211-23C>A	NP_001336875.1:n.-211-23C>A
NM_001349947.1:c.-234C>A	NP_001336876.1:n.-234C>A
NM_001349946.2:c.-211-23C>A	NP_001336875.1:n.-211-23C>A
NM_001349947.2:c.-234C>A	NP_001336876.1:n.-234C>A