Canonical Allele Identifier: CA2260738807

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998789C= , CM000679.2:g.42998789C=	GRCh38
NC_000017.10:g.41150806C= , CM000679.1:g.41150806C=	GRCh37
NC_000017.9:g.38404332C=	NCBI36
NG_053099.1:g.5517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.39C= MANE Select	ENSP00000253788.5:p.Val13=
ENST00000589913.6:c.39C=	ENSP00000464813.1:p.Val13=
ENST00000590864.2:c.39C=	ENSP00000467939.2:p.Val13=
ENST00000253788.9:c.39C=	ENSP00000253788.4:p.Val13=
ENST00000587478.1:n.94C=
ENST00000588830.1:c.39C=	ENSP00000468468.1:p.Val13=
ENST00000589037.5:c.39C=	ENSP00000467587.1:p.Val13=
ENST00000589913.5:c.39C=	ENSP00000464813.1:p.Val13=
ENST00000593262.1:n.371C=
NM_000988.3:c.39C=	NP_000979.1:p.Val13=
NM_000988.5:c.39C= MANE Select	NP_000979.1:p.Val13=
NM_001349921.1:c.39C=	NP_001336850.1:p.Val13=
NM_001349922.1:c.39C=	NP_001336851.1:p.Val13=
NR_146327.1:n.122C=
NM_001349921.2:c.39C=	NP_001336850.1:p.Val13=
NM_001349922.2:c.39C=	NP_001336851.1:p.Val13=
NR_146327.2:n.94C=