Canonical Allele Identifier: CA350314387

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201633433T>C , CM000664.2:g.201633433T>C	GRCh38
NC_000002.11:g.202498156T>C , CM000664.1:g.202498156T>C	GRCh37
NC_000002.10:g.202206401T>C	NCBI36
NG_032049.1:g.15097A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.275-2A>G MANE Select	NP_001037850.1:n.275-2A>G
ENST00000409883.7:c.275-2A>G MANE Select	ENSP00000386264.2:n.275-2A>G
NM_001044385.2:c.275-2A>G	NP_001037850.1:n.275-2A>G
NM_152388.3:c.251-2A>G	NP_689601.2:n.251-2A>G
NM_152388.4:c.251-2A>G	NP_689601.2:n.251-2A>G
ENST00000286196.9:c.196-2A>G	ENSP00000286196.5:n.196-2A>G
ENST00000409444.6:c.251-2A>G	ENSP00000387203.2:n.251-2A>G
ENST00000409883.6:c.275-2A>G	ENSP00000386264.2:n.275-2A>G
ENST00000432684.6:c.*74-2A>G	ENSP00000413230.2:n.*74-2A>G
ENST00000444047.6:c.*85-2A>G	ENSP00000402681.2:n.*85-2A>G
ENST00000471318.6:n.165-2A>G
ENST00000489550.5:n.378-2A>G
ENST00000621467.4:c.251-2A>G	ENSP00000480508.1:n.251-2A>G
ENST00000621467.5:c.149-2A>G	ENSP00000480508.2:n.149-2A>G
ENST00000686475.1:n.111-2A>G