Canonical Allele Identifier: CA2753881179

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626291_201626303del , CM000664.2:g.201626291_201626303del	GRCh38
NC_000002.11:g.202491014_202491026del , CM000664.1:g.202491014_202491026del	GRCh37
NC_000002.10:g.202199259_202199271del	NCBI36
NG_032049.1:g.22229_22241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-154_834-142del
ENST00000621467.5:c.912-154_912-142del	ENSP00000480508.2:n.912-154_912-142del
ENST00000686475.1:n.978-154_978-142del
ENST00000409883.7:c.1038-154_1038-142del MANE Select	ENSP00000386264.2:n.1038-154_1038-142del
ENST00000286196.9:c.*602-154_*602-142del	ENSP00000286196.5:n.*602-154_*602-142del
ENST00000409444.6:c.1014-154_1014-142del	ENSP00000387203.2:n.1014-154_1014-142del
ENST00000409883.6:c.1038-154_1038-142del	ENSP00000386264.2:n.1038-154_1038-142del
ENST00000471318.5:n.266-154_266-142del
ENST00000495329.1:n.23_35del
ENST00000621467.4:c.1014-154_1014-142del	ENSP00000480508.1:n.1014-154_1014-142del
NM_001044385.2:c.1038-154_1038-142del	NP_001037850.1:n.1038-154_1038-142del
NM_152388.3:c.1014-154_1014-142del	NP_689601.2:n.1014-154_1014-142del
NM_001044385.3:c.1038-154_1038-142del MANE Select	NP_001037850.1:n.1038-154_1038-142del
NM_152388.4:c.1014-154_1014-142del	NP_689601.2:n.1014-154_1014-142del