Canonical Allele Identifier: CA2638053595

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998673-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998673T>C , CM000679.2:g.42998673T>C	GRCh38
NC_000017.10:g.41150690T>C , CM000679.1:g.41150690T>C	GRCh37
NC_000017.9:g.38404216T>C	NCBI36
NG_053099.1:g.5401T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000253788.12:c.-2-76T>C MANE Select	ENSP00000253788.5:n.-2-76T>C
ENST00000589913.6:c.-78T>C	ENSP00000464813.1:n.-78T>C
ENST00000253788.9:c.-2-76T>C	ENSP00000253788.4:n.-2-76T>C
ENST00000587478.1:n.54-76T>C
ENST00000588830.1:c.-2-76T>C	ENSP00000468468.1:n.-2-76T>C
ENST00000589037.5:c.-2-76T>C	ENSP00000467587.1:n.-2-76T>C
ENST00000589913.5:c.-78T>C	ENSP00000464813.1:n.-78T>C
ENST00000593262.1:n.255T>C
NM_000988.3:c.-2-76T>C	NP_000979.1:n.-2-76T>C
NM_000988.5:c.-2-76T>C MANE Select	NP_000979.1:n.-2-76T>C
NM_001349921.1:c.-2-76T>C	NP_001336850.1:n.-2-76T>C
NM_001349922.1:c.-78T>C	NP_001336851.1:n.-78T>C
NR_146327.1:n.82-76T>C
NM_001349921.2:c.-2-76T>C	NP_001336850.1:n.-2-76T>C
NM_001349922.2:c.-78T>C	NP_001336851.1:n.-78T>C
NR_146327.2:n.54-76T>C