Canonical Allele Identifier: CA2638054534

Gene: RPL27

Linked Data

• gnomAD v4: 17-42999060-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999060A>C , CM000679.2:g.42999060A>C	GRCh38
NC_000017.10:g.41151077A>C , CM000679.1:g.41151077A>C	GRCh37
NC_000017.9:g.38404603A>C	NCBI36
NG_053099.1:g.5788A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+229A>C MANE Select	ENSP00000253788.5:n.81+229A>C
ENST00000589913.6:c.81+229A>C	ENSP00000464813.1:n.81+229A>C
ENST00000590864.2:c.82-126A>C	ENSP00000467939.2:n.82-126A>C
ENST00000253788.9:c.81+229A>C	ENSP00000253788.4:n.81+229A>C
ENST00000586277.5:c.104+148A>C
ENST00000587478.1:n.365A>C
ENST00000588830.1:c.81+229A>C	ENSP00000468468.1:n.81+229A>C
ENST00000589037.5:c.81+229A>C	ENSP00000467587.1:n.81+229A>C
ENST00000589913.5:c.81+229A>C	ENSP00000464813.1:n.81+229A>C
ENST00000593262.1:n.642A>C
NM_000988.3:c.81+229A>C	NP_000979.1:n.81+229A>C
NM_000988.5:c.81+229A>C MANE Select	NP_000979.1:n.81+229A>C
NM_001349921.1:c.81+229A>C	NP_001336850.1:n.81+229A>C
NM_001349922.1:c.81+229A>C	NP_001336851.1:n.81+229A>C
NR_146327.1:n.164+229A>C
NM_001349921.2:c.81+229A>C	NP_001336850.1:n.81+229A>C
NM_001349922.2:c.81+229A>C	NP_001336851.1:n.81+229A>C
NR_146327.2:n.136+229A>C