Canonical Allele Identifier: CA2662657521

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201625917-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625918dup , CM000664.2:g.201625918dup	GRCh38
NC_000002.11:g.202490641dup , CM000664.1:g.202490641dup	GRCh37
NC_000002.10:g.202198886dup	NCBI36
NG_032049.1:g.22612dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+108dup
ENST00000621467.5:c.1033+108dup	ENSP00000480508.2:n.1033+108dup
ENST00000686475.1:n.1099+108dup
ENST00000409883.7:c.1159+108dup MANE Select	ENSP00000386264.2:n.1159+108dup
ENST00000286196.9:c.*723+108dup	ENSP00000286196.5:n.*723+108dup
ENST00000409444.6:c.1135+108dup	ENSP00000387203.2:n.1135+108dup
ENST00000409883.6:c.1159+108dup	ENSP00000386264.2:n.1159+108dup
ENST00000471318.5:n.387+108dup
ENST00000495329.1:n.298+108dup
ENST00000621467.4:c.1135+108dup	ENSP00000480508.1:n.1135+108dup
NM_001044385.2:c.1159+108dup	NP_001037850.1:n.1159+108dup
NM_152388.3:c.1135+108dup	NP_689601.2:n.1135+108dup
NM_001044385.3:c.1159+108dup MANE Select	NP_001037850.1:n.1159+108dup
NM_152388.4:c.1135+108dup	NP_689601.2:n.1135+108dup