Canonical Allele Identifier: CA2638053575

Gene: RPL27

Linked Data

• dbSNP Id: rs2151964425
• gnomAD v4: 17-42998660-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998660C>G , CM000679.2:g.42998660C>G	GRCh38
NC_000017.10:g.41150677C>G , CM000679.1:g.41150677C>G	GRCh37
NC_000017.9:g.38404203C>G	NCBI36
NG_053099.1:g.5388C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000253788.12:c.-2-89C>G MANE Select	ENSP00000253788.5:n.-2-89C>G
ENST00000589913.6:c.-91C>G	ENSP00000464813.1:n.-91C>G
ENST00000253788.9:c.-2-89C>G	ENSP00000253788.4:n.-2-89C>G
ENST00000587478.1:n.54-89C>G
ENST00000588830.1:c.-2-89C>G	ENSP00000468468.1:n.-2-89C>G
ENST00000589037.5:c.-2-89C>G	ENSP00000467587.1:n.-2-89C>G
ENST00000589913.5:c.-91C>G	ENSP00000464813.1:n.-91C>G
ENST00000593262.1:n.242C>G
NM_000988.3:c.-2-89C>G	NP_000979.1:n.-2-89C>G
NM_000988.5:c.-2-89C>G MANE Select	NP_000979.1:n.-2-89C>G
NM_001349921.1:c.-2-89C>G	NP_001336850.1:n.-2-89C>G
NM_001349922.1:c.-91C>G	NP_001336851.1:n.-91C>G
NR_146327.1:n.82-89C>G
NM_001349921.2:c.-2-89C>G	NP_001336850.1:n.-2-89C>G
NM_001349922.2:c.-91C>G	NP_001336851.1:n.-91C>G
NR_146327.2:n.54-89C>G