Canonical Allele Identifier: CA2638053266

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998531-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998531A>C , CM000679.2:g.42998531A>C	GRCh38
NC_000017.10:g.41150548A>C , CM000679.1:g.41150548A>C	GRCh37
NC_000017.9:g.38404074A>C	NCBI36
NG_053099.1:g.5259A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+60A>C MANE Select	ENSP00000253788.5:n.-3+60A>C
ENST00000589913.6:c.-220A>C	ENSP00000464813.1:n.-220A>C
ENST00000253788.9:c.-3+60A>C	ENSP00000253788.4:n.-3+60A>C
ENST00000587478.1:n.53+60A>C
ENST00000588830.1:c.-3+60A>C	ENSP00000468468.1:n.-3+60A>C
ENST00000589037.5:c.-3+116A>C	ENSP00000467587.1:n.-3+116A>C
ENST00000589913.5:c.-220A>C	ENSP00000464813.1:n.-220A>C
ENST00000593262.1:n.113A>C
NM_000988.3:c.-3+60A>C	NP_000979.1:n.-3+60A>C
NM_000988.5:c.-3+60A>C MANE Select	NP_000979.1:n.-3+60A>C
NM_001349921.1:c.-3+116A>C	NP_001336850.1:n.-3+116A>C
NM_001349922.1:c.-220A>C	NP_001336851.1:n.-220A>C
NR_146327.1:n.81+60A>C
NM_001349921.2:c.-3+116A>C	NP_001336850.1:n.-3+116A>C
NM_001349922.2:c.-220A>C	NP_001336851.1:n.-220A>C
NR_146327.2:n.53+60A>C