Canonical Allele Identifier: CA2662662844

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201640224-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640224G>T , CM000664.2:g.201640224G>T	GRCh38
NC_000002.11:g.202504947G>T , CM000664.1:g.202504947G>T	GRCh37
NC_000002.10:g.202213192G>T	NCBI36
NG_032049.1:g.8306C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+669C>A	ENSP00000480508.2:n.-356+669C>A
ENST00000409883.7:c.79+37C>A MANE Select	ENSP00000386264.2:n.79+37C>A
ENST00000286196.9:c.-1+669C>A	ENSP00000286196.5:n.-1+669C>A
ENST00000409444.6:c.55+37C>A	ENSP00000387203.2:n.55+37C>A
ENST00000409883.6:c.79+37C>A	ENSP00000386264.2:n.79+37C>A
ENST00000432684.6:c.79+37C>A	ENSP00000413230.2:n.79+37C>A
ENST00000444047.6:c.79+37C>A	ENSP00000402681.2:n.79+37C>A
ENST00000463205.2:n.82+37C>A
ENST00000489550.5:n.92+669C>A
ENST00000621467.4:c.50+669C>A	ENSP00000480508.1:n.50+669C>A
NM_001044385.2:c.79+37C>A	NP_001037850.1:n.79+37C>A
NM_152388.3:c.55+37C>A	NP_689601.2:n.55+37C>A
NM_001044385.3:c.79+37C>A MANE Select	NP_001037850.1:n.79+37C>A
NM_152388.4:c.55+37C>A	NP_689601.2:n.55+37C>A