Canonical Allele Identifier: CA2662657028

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201623494-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623494A>C , CM000664.2:g.201623494A>C	GRCh38
NC_000002.11:g.202488217A>C , CM000664.1:g.202488217A>C	GRCh37
NC_000002.10:g.202196462A>C	NCBI36
NG_032049.1:g.25036T>G
NG_051007.1:g.689T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*761T>G	ENSP00000480508.2:n.*761T>G
ENST00000686475.1:n.1928T>G
ENST00000409883.7:c.*761T>G MANE Select	ENSP00000386264.2:n.*761T>G
ENST00000409444.6:c.*761T>G	ENSP00000387203.2:n.*761T>G
ENST00000409883.6:c.*761T>G	ENSP00000386264.2:n.*761T>G
ENST00000495329.1:n.1127T>G
NM_001044385.2:c.*761T>G	NP_001037850.1:n.*761T>G
NM_152388.3:c.*761T>G	NP_689601.2:n.*761T>G
NM_001044385.3:c.*761T>G MANE Select	NP_001037850.1:n.*761T>G
NM_152388.4:c.*761T>G	NP_689601.2:n.*761T>G