Canonical Allele Identifier: CA2056521

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201633409T>C , CM000664.2:g.201633409T>C	GRCh38
NC_000002.11:g.202498132T>C , CM000664.1:g.202498132T>C	GRCh37
NC_000002.10:g.202206377T>C	NCBI36
NG_032049.1:g.15121A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.297A>G MANE Select	NP_001037850.1:p.Gln99=
ENST00000409883.7:c.297A>G MANE Select	ENSP00000386264.2:p.Gln99=
NM_001044385.2:c.297A>G	NP_001037850.1:p.Gln99=
NM_152388.3:c.273A>G	NP_689601.2:p.Gln91=
NM_152388.4:c.273A>G	NP_689601.2:p.Gln91=
ENST00000286196.9:c.218A>G	ENSP00000286196.5:p.Lys73Arg
ENST00000409444.6:c.273A>G	ENSP00000387203.2:p.Gln91=
ENST00000409883.6:c.297A>G	ENSP00000386264.2:p.Gln99=
ENST00000432684.6:c.*96A>G	ENSP00000413230.2:n.*96A>G
ENST00000444047.6:c.*107A>G	ENSP00000402681.2:n.*107A>G
ENST00000471318.6:n.187A>G
ENST00000489550.5:n.400A>G
ENST00000621467.4:c.273A>G	ENSP00000480508.1:p.Gln91=
ENST00000621467.5:c.171A>G	ENSP00000480508.2:p.Gln57=
ENST00000686475.1:n.133A>G