Canonical Allele Identifier: CA65638868

Gene: RPL37A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216499955A>G , CM000664.2:g.216499955A>G	GRCh38
NC_000002.11:g.217364678A>G , CM000664.1:g.217364678A>G	GRCh37
NC_000002.10:g.217072923A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000998.5:c.139A>G MANE Select	NP_000989.1:p.Met47Val
ENST00000491306.6:c.139A>G MANE Select	ENSP00000418082.1:p.Met47Val
NM_000998.4:c.139A>G	NP_000989.1:p.Met47Val
ENST00000359681.3:n.539A>G
ENST00000420712.1:c.174A>G	ENSP00000410080.1:p.Arg58=
ENST00000427280.6:c.67A>G	ENSP00000472653.1:p.Met23Val
ENST00000441179.2:c.67A>G	ENSP00000471102.1:p.Met23Val
ENST00000446558.5:c.139A>G	ENSP00000388690.1:p.Met47Val
ENST00000456586.5:c.67A>G	ENSP00000410240.1:p.Met23Val
ENST00000478153.1:n.581A>G
ENST00000487233.1:n.720A>G
ENST00000490649.1:n.189A>G
ENST00000491306.5:c.139A>G	ENSP00000418082.1:p.Met47Val
ENST00000598925.5:c.67A>G	ENSP00000469607.1:p.Met23Val
ENST00000600880.5:c.139A>G	ENSP00000470348.1:p.Met47Val