Canonical Allele Identifier: CA2056553

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201636839G>A , CM000664.2:g.201636839G>A	GRCh38
NC_000002.11:g.202501562G>A , CM000664.1:g.202501562G>A	GRCh37
NC_000002.10:g.202209807G>A	NCBI36
NG_032049.1:g.11691C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.183C>T MANE Select	NP_001037850.1:p.Pro61=
ENST00000409883.7:c.183C>T MANE Select	ENSP00000386264.2:p.Pro61=
NM_001044385.2:c.183C>T	NP_001037850.1:p.Pro61=
NM_152388.3:c.159C>T	NP_689601.2:p.Pro53=
NM_152388.4:c.159C>T	NP_689601.2:p.Pro53=
ENST00000286196.9:c.104C>T	ENSP00000286196.5:p.Pro35Leu
ENST00000409444.6:c.159C>T	ENSP00000387203.2:p.Pro53=
ENST00000409883.6:c.183C>T	ENSP00000386264.2:p.Pro61=
ENST00000432684.6:c.183C>T	ENSP00000413230.2:p.Pro61=
ENST00000444047.6:c.183C>T	ENSP00000402681.2:p.Pro61=
ENST00000471318.6:n.73C>T
ENST00000480124.1:n.90C>T
ENST00000489550.5:n.196C>T
ENST00000621467.4:c.159C>T	ENSP00000480508.1:p.Pro53=
ENST00000621467.5:c.57C>T	ENSP00000480508.2:p.Pro19=
ENST00000686475.1:n.19C>T