Canonical Allele Identifier: CA2662657011

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201623461-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623461C>A , CM000664.2:g.201623461C>A	GRCh38
NC_000002.11:g.202488184C>A , CM000664.1:g.202488184C>A	GRCh37
NC_000002.10:g.202196429C>A	NCBI36
NG_032049.1:g.25069G>T
NG_051007.1:g.722G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*794G>T	ENSP00000480508.2:n.*794G>T
ENST00000686475.1:n.1961G>T
ENST00000409883.7:c.*794G>T MANE Select	ENSP00000386264.2:n.*794G>T
ENST00000409444.6:c.*794G>T	ENSP00000387203.2:n.*794G>T
ENST00000409883.6:c.*794G>T	ENSP00000386264.2:n.*794G>T
ENST00000495329.1:n.1160G>T
NM_001044385.2:c.*794G>T	NP_001037850.1:n.*794G>T
NM_152388.3:c.*794G>T	NP_689601.2:n.*794G>T
NM_001044385.3:c.*794G>T MANE Select	NP_001037850.1:n.*794G>T
NM_152388.4:c.*794G>T	NP_689601.2:n.*794G>T