Canonical Allele Identifier: CA2753881187

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626394_201626398del , CM000664.2:g.201626394_201626398del	GRCh38
NC_000002.11:g.202491117_202491121del , CM000664.1:g.202491117_202491121del	GRCh37
NC_000002.10:g.202199362_202199366del	NCBI36
NG_032049.1:g.22132_22136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-251_834-247del
ENST00000621467.5:c.912-251_912-247del	ENSP00000480508.2:n.912-251_912-247del
ENST00000686475.1:n.978-251_978-247del
ENST00000409883.7:c.1038-251_1038-247del MANE Select	ENSP00000386264.2:n.1038-251_1038-247del
ENST00000286196.9:c.*602-251_*602-247del	ENSP00000286196.5:n.*602-251_*602-247del
ENST00000409444.6:c.1014-251_1014-247del	ENSP00000387203.2:n.1014-251_1014-247del
ENST00000409883.6:c.1038-251_1038-247del	ENSP00000386264.2:n.1038-251_1038-247del
ENST00000471318.5:n.266-251_266-247del
ENST00000621467.4:c.1014-251_1014-247del	ENSP00000480508.1:n.1014-251_1014-247del
NM_001044385.2:c.1038-251_1038-247del	NP_001037850.1:n.1038-251_1038-247del
NM_152388.3:c.1014-251_1014-247del	NP_689601.2:n.1014-251_1014-247del
NM_001044385.3:c.1038-251_1038-247del MANE Select	NP_001037850.1:n.1038-251_1038-247del
NM_152388.4:c.1014-251_1014-247del	NP_689601.2:n.1014-251_1014-247del