Canonical Allele Identifier: CA2638052896

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998467-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998467T>C , CM000679.2:g.42998467T>C	GRCh38
NC_000017.10:g.41150484T>C , CM000679.1:g.41150484T>C	GRCh37
NC_000017.9:g.38404010T>C	NCBI36
NG_053099.1:g.5195T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-7T>C MANE Select	ENSP00000253788.5:n.-7T>C
ENST00000253788.9:c.-7T>C	ENSP00000253788.4:n.-7T>C
ENST00000587478.1:n.49T>C
ENST00000588830.1:c.-7T>C	ENSP00000468468.1:n.-7T>C
ENST00000589037.5:c.-3+52T>C	ENSP00000467587.1:n.-3+52T>C
ENST00000593262.1:n.49T>C
NM_000988.3:c.-7T>C	NP_000979.1:n.-7T>C
NM_000988.5:c.-7T>C MANE Select	NP_000979.1:n.-7T>C
NM_001349921.1:c.-3+52T>C	NP_001336850.1:n.-3+52T>C
NM_001349922.1:c.-284T>C	NP_001336851.1:n.-284T>C
NR_146327.1:n.77T>C
NM_001349921.2:c.-3+52T>C	NP_001336850.1:n.-3+52T>C
NM_001349922.2:c.-284T>C	NP_001336851.1:n.-284T>C
NR_146327.2:n.49T>C