Canonical Allele Identifier: CA626076685

Gene: RPL27

Linked Data

• dbSNP Id: rs1424411389
• gnomAD v2: 17-41150741-G-A
• gnomAD v4: 17-42998724-G-A
• MyVariant Identifiers: chr17:g.41150741G>A (hg19) ; chr17:g.42998724G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998724G>A , CM000679.2:g.42998724G>A	GRCh38
NC_000017.10:g.41150741G>A , CM000679.1:g.41150741G>A	GRCh37
NC_000017.9:g.38404267G>A	NCBI36
NG_053099.1:g.5452G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-2-25G>A MANE Select	ENSP00000253788.5:n.-2-25G>A
ENST00000589913.6:c.-27G>A	ENSP00000464813.1:n.-27G>A
ENST00000590864.2:c.-27G>A	ENSP00000467939.2:n.-27G>A
ENST00000253788.9:c.-2-25G>A	ENSP00000253788.4:n.-2-25G>A
ENST00000587478.1:n.54-25G>A
ENST00000588830.1:c.-2-25G>A	ENSP00000468468.1:n.-2-25G>A
ENST00000589037.5:c.-2-25G>A	ENSP00000467587.1:n.-2-25G>A
ENST00000589913.5:c.-27G>A	ENSP00000464813.1:n.-27G>A
ENST00000593262.1:n.306G>A
NM_000988.3:c.-2-25G>A	NP_000979.1:n.-2-25G>A
NM_000988.5:c.-2-25G>A MANE Select	NP_000979.1:n.-2-25G>A
NM_001349921.1:c.-2-25G>A	NP_001336850.1:n.-2-25G>A
NM_001349922.1:c.-27G>A	NP_001336851.1:n.-27G>A
NR_146327.1:n.82-25G>A
NM_001349921.2:c.-2-25G>A	NP_001336850.1:n.-2-25G>A
NM_001349922.2:c.-27G>A	NP_001336851.1:n.-27G>A
NR_146327.2:n.54-25G>A