Canonical Allele Identifier: CA2753881143
Gene: TMEM237 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626239_201626241del , CM000664.2:g.201626239_201626241del GRCh38
NC_000002.11:g.202490962_202490964del , CM000664.1:g.202490962_202490964del GRCh37
NC_000002.10:g.202199207_202199209del NCBI36
NG_032049.1:g.22289_22291del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471318.6:n.834-94_834-92del
ENST00000621467.5:c.912-94_912-92del ENSP00000480508.2:n.912-94_912-92del
ENST00000686475.1:n.978-94_978-92del
ENST00000409883.7:c.1038-94_1038-92del MANE Select ENSP00000386264.2:n.1038-94_1038-92del
ENST00000286196.9:c.*602-94_*602-92del ENSP00000286196.5:n.*602-94_*602-92del
ENST00000409444.6:c.1014-94_1014-92del ENSP00000387203.2:n.1014-94_1014-92del
ENST00000409883.6:c.1038-94_1038-92del ENSP00000386264.2:n.1038-94_1038-92del
ENST00000471318.5:n.266-94_266-92del
ENST00000495329.1:n.83_85del
ENST00000621467.4:c.1014-94_1014-92del ENSP00000480508.1:n.1014-94_1014-92del
NM_001044385.2:c.1038-94_1038-92del NP_001037850.1:n.1038-94_1038-92del
NM_152388.3:c.1014-94_1014-92del NP_689601.2:n.1014-94_1014-92del
NM_001044385.3:c.1038-94_1038-92del MANE Select NP_001037850.1:n.1038-94_1038-92del
NM_152388.4:c.1014-94_1014-92del NP_689601.2:n.1014-94_1014-92del
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