Canonical Allele Identifier: CA399675789

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150794G>C (hg19) ; chr17:g.42998777G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998777G>C , CM000679.2:g.42998777G>C	GRCh38
NC_000017.10:g.41150794G>C , CM000679.1:g.41150794G>C	GRCh37
NC_000017.9:g.38404320G>C	NCBI36
NG_053099.1:g.5505G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.27G>C MANE Select	ENSP00000253788.5:p.Lys9Asn
ENST00000589913.6:c.27G>C	ENSP00000464813.1:p.Lys9Asn
ENST00000590864.2:c.27G>C	ENSP00000467939.2:p.Lys9Asn
ENST00000253788.9:c.27G>C	ENSP00000253788.4:p.Lys9Asn
ENST00000587478.1:n.82G>C
ENST00000588830.1:c.27G>C	ENSP00000468468.1:p.Lys9Asn
ENST00000589037.5:c.27G>C	ENSP00000467587.1:p.Lys9Asn
ENST00000589913.5:c.27G>C	ENSP00000464813.1:p.Lys9Asn
ENST00000593262.1:n.359G>C
NM_000988.3:c.27G>C	NP_000979.1:p.Lys9Asn
NM_000988.5:c.27G>C MANE Select	NP_000979.1:p.Lys9Asn
NM_001349921.1:c.27G>C	NP_001336850.1:p.Lys9Asn
NM_001349922.1:c.27G>C	NP_001336851.1:p.Lys9Asn
NR_146327.1:n.110G>C
NM_001349921.2:c.27G>C	NP_001336850.1:p.Lys9Asn
NM_001349922.2:c.27G>C	NP_001336851.1:p.Lys9Asn
NR_146327.2:n.82G>C