Canonical Allele Identifier: CA505179917

Gene: RPL36

Linked Data

• MyVariant Identifiers: chr19:g.5691581G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691570G>A , CM000681.2:g.5691570G>A	GRCh38
NC_000019.9:g.5691581G>A , CM000681.1:g.5691581G>A	GRCh37
NC_000019.8:g.5642581G>A	NCBI36
NG_017015.1:g.6310G>A
NG_033142.1:g.33883C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.267G>A MANE Select	ENSP00000252543.3:p.Glu89=
ENST00000347512.7:c.267G>A	ENSP00000252543.3:p.Glu89=
ENST00000394580.2:c.267G>A	ENSP00000378081.2:p.Glu89=
ENST00000577222.5:c.267G>A	ENSP00000464342.1:p.Glu89=
ENST00000579446.1:c.*60G>A	ENSP00000464613.1:n.*60G>A
ENST00000579649.5:c.267G>A	ENSP00000462609.1:p.Glu89=
NM_015414.3:c.267G>A	NP_056229.2:p.Glu89=
NM_033643.2:c.267G>A	NP_378669.1:p.Glu89=
NM_033643.3:c.267G>A MANE Select	NP_378669.1:p.Glu89=
NM_015414.4:c.267G>A	NP_056229.2:p.Glu89=