Canonical Allele Identifier: CA333091311

Gene: RPL36A RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101391167A>G , CM000685.2:g.101391167A>G	GRCh38
NC_000023.10:g.100646155A>G , CM000685.1:g.100646155A>G	GRCh37
NC_000023.9:g.100532811A>G	NCBI36
NG_009616.1:g.58T>C , LRG_128:g.58T>C
NG_012523.1:g.5208A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021029.6:c.3+121A>G (RPL36A) MANE Select	NP_066357.3:n.3+121A>G
ENST00000553110.8:c.3+121A>G (RPL36A) MANE Select	ENSP00000446503.2:n.3+121A>G
NM_001199972.1:c.111+121A>G (RPL36A)	NP_001186901.1:n.111+121A>G
NM_001199973.1:c.111+121A>G (RPL36A-HNRNPH2)	NP_001186902.1:n.111+121A>G
NM_001199973.2:c.3+121A>G (RPL36A-HNRNPH2)	NP_001186902.2:n.3+121A>G
NM_001199974.1:c.111+121A>G (RPL36A-HNRNPH2)	NP_001186903.1:n.111+121A>G
NM_001199974.2:c.3+121A>G (RPL36A-HNRNPH2)	NP_001186903.2:n.3+121A>G
NM_021029.5:c.111+121A>G (RPL36A)	NP_066357.2:n.111+121A>G
ENST00000372849.8:c.3+121A>G (RPL36A)	ENSP00000361940.5:n.3+121A>G
ENST00000392994.7:c.3+121A>G (RPL36A)	ENSP00000397659.3:n.3+121A>G
ENST00000409170.3:c.3+121A>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.3+121A>G
ENST00000409338.5:c.3+121A>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.3+121A>G
ENST00000427805.6:c.111+121A>G (RPL36A)	ENSP00000404375.2:n.111+121A>G
ENST00000465340.5:n.36+121A>G (RPL36A)
ENST00000465744.5:n.54A>G (RPL36A)
ENST00000491851.5:n.36+121A>G (RPL36A)
ENST00000553110.7:c.3+121A>G (RPL36A)	ENSP00000446503.1:n.3+121A>G
ENST00000614077.4:c.111+121A>G (RPL36A)	ENSP00000483017.1:n.111+121A>G