Canonical Allele Identifier: CA399675920

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150833A>T (hg19) ; chr17:g.42998816A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998816A>T , CM000679.2:g.42998816A>T	GRCh38
NC_000017.10:g.41150833A>T , CM000679.1:g.41150833A>T	GRCh37
NC_000017.9:g.38404359A>T	NCBI36
NG_053099.1:g.5544A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.66A>T MANE Select	ENSP00000253788.5:p.Lys22Asn
ENST00000589913.6:c.66A>T	ENSP00000464813.1:p.Lys22Asn
ENST00000590864.2:c.66A>T	ENSP00000467939.2:p.Lys22Asn
ENST00000253788.9:c.66A>T	ENSP00000253788.4:p.Lys22Asn
ENST00000586277.5:c.8A>T
ENST00000587478.1:n.121A>T
ENST00000588830.1:c.66A>T	ENSP00000468468.1:p.Lys22Asn
ENST00000589037.5:c.66A>T	ENSP00000467587.1:p.Lys22Asn
ENST00000589913.5:c.66A>T	ENSP00000464813.1:p.Lys22Asn
ENST00000593262.1:n.398A>T
NM_000988.3:c.66A>T	NP_000979.1:p.Lys22Asn
NM_000988.5:c.66A>T MANE Select	NP_000979.1:p.Lys22Asn
NM_001349921.1:c.66A>T	NP_001336850.1:p.Lys22Asn
NM_001349922.1:c.66A>T	NP_001336851.1:p.Lys22Asn
NR_146327.1:n.149A>T
NM_001349921.2:c.66A>T	NP_001336850.1:p.Lys22Asn
NM_001349922.2:c.66A>T	NP_001336851.1:p.Lys22Asn
NR_146327.2:n.121A>T