Canonical Allele Identifier: CA2558157352

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623472del , CM000664.2:g.201623472del	GRCh38
NC_000002.11:g.202488195del , CM000664.1:g.202488195del	GRCh37
NC_000002.10:g.202196440del	NCBI36
NG_032049.1:g.25060del
NG_051007.1:g.713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*785del	ENSP00000480508.2:n.*785del
ENST00000686475.1:n.1952del
ENST00000409883.7:c.*785del MANE Select	ENSP00000386264.2:n.*785del
ENST00000409444.6:c.*785del	ENSP00000387203.2:n.*785del
ENST00000409883.6:c.*785del	ENSP00000386264.2:n.*785del
ENST00000495329.1:n.1151del
NM_001044385.2:c.*785del	NP_001037850.1:n.*785del
NM_152388.3:c.*785del	NP_689601.2:n.*785del
NM_001044385.3:c.*785del MANE Select	NP_001037850.1:n.*785del
NM_152388.4:c.*785del	NP_689601.2:n.*785del