Canonical Allele Identifier: CA3096594028

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201629694A= , CM000664.2:g.201629694A=	GRCh38
NC_000002.11:g.202494417A= , CM000664.1:g.202494417A=	GRCh37
NC_000002.10:g.202202662A=	NCBI36
NG_032049.1:g.18836T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.677+35T= MANE Select	NP_001037850.1:n.677+35T=
ENST00000409883.7:c.677+35T= MANE Select	ENSP00000386264.2:n.677+35T=
NM_001044385.2:c.677+35T=	NP_001037850.1:n.677+35T=
NM_152388.3:c.653+35T=	NP_689601.2:n.653+35T=
NM_152388.4:c.653+35T=	NP_689601.2:n.653+35T=
ENST00000286196.9:c.*241+35T=	ENSP00000286196.5:n.*241+35T=
ENST00000409444.6:c.653+35T=	ENSP00000387203.2:n.653+35T=
ENST00000409883.6:c.677+35T=	ENSP00000386264.2:n.677+35T=
ENST00000432684.6:c.*476+35T=	ENSP00000413230.2:n.*476+35T=
ENST00000466641.5:n.375+35T=
ENST00000466839.5:n.545+35T=
ENST00000471318.6:n.567+35T=
ENST00000621467.4:c.653+35T=	ENSP00000480508.1:n.653+35T=
ENST00000621467.5:c.551+35T=	ENSP00000480508.2:n.551+35T=
ENST00000686475.1:n.617+35T=