Canonical Allele Identifier: CA2638053252

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998527-TCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998528_42998529del , CM000679.2:g.42998528_42998529del	GRCh38
NC_000017.10:g.41150545_41150546del , CM000679.1:g.41150545_41150546del	GRCh37
NC_000017.9:g.38404071_38404072del	NCBI36
NG_053099.1:g.5256_5257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+57_-3+58del MANE Select	ENSP00000253788.5:n.-3+57_-3+58del
ENST00000589913.6:c.-223_-222del	ENSP00000464813.1:n.-223_-222del
ENST00000253788.9:c.-3+57_-3+58del	ENSP00000253788.4:n.-3+57_-3+58del
ENST00000587478.1:n.53+57_53+58del
ENST00000588830.1:c.-3+57_-3+58del	ENSP00000468468.1:n.-3+57_-3+58del
ENST00000589037.5:c.-3+113_-3+114del	ENSP00000467587.1:n.-3+113_-3+114del
ENST00000589913.5:c.-223_-222del	ENSP00000464813.1:n.-223_-222del
ENST00000593262.1:n.110_111del
NM_000988.3:c.-3+57_-3+58del	NP_000979.1:n.-3+57_-3+58del
NM_000988.5:c.-3+57_-3+58del MANE Select	NP_000979.1:n.-3+57_-3+58del
NM_001349921.1:c.-3+113_-3+114del	NP_001336850.1:n.-3+113_-3+114del
NM_001349922.1:c.-223_-222del	NP_001336851.1:n.-223_-222del
NR_146327.1:n.81+57_81+58del
NM_001349921.2:c.-3+113_-3+114del	NP_001336850.1:n.-3+113_-3+114del
NM_001349922.2:c.-223_-222del	NP_001336851.1:n.-223_-222del
NR_146327.2:n.53+57_53+58del