Canonical Allele Identifier: CA403524071

Gene: RPL36

Linked Data

• MyVariant Identifiers: chr19:g.5691569G>T (hg19) ; chr19:g.5691558G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691558G>T , CM000681.2:g.5691558G>T	GRCh38
NC_000019.9:g.5691569G>T , CM000681.1:g.5691569G>T	GRCh37
NC_000019.8:g.5642569G>T	NCBI36
NG_017015.1:g.6298G>T
NG_033142.1:g.33895C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.255G>T MANE Select	ENSP00000252543.3:p.Arg85Ser
ENST00000347512.7:c.255G>T	ENSP00000252543.3:p.Arg85Ser
ENST00000394580.2:c.255G>T	ENSP00000378081.2:p.Arg85Ser
ENST00000577222.5:c.255G>T	ENSP00000464342.1:p.Arg85Ser
ENST00000579446.1:c.*48G>T	ENSP00000464613.1:n.*48G>T
ENST00000579649.5:c.255G>T	ENSP00000462609.1:p.Arg85Ser
NM_015414.3:c.255G>T	NP_056229.2:p.Arg85Ser
NM_033643.2:c.255G>T	NP_378669.1:p.Arg85Ser
NM_033643.3:c.255G>T MANE Select	NP_378669.1:p.Arg85Ser
NM_015414.4:c.255G>T	NP_056229.2:p.Arg85Ser