Canonical Allele Identifier: CA2753881151
Gene: TMEM237 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626242_201626248del , CM000664.2:g.201626242_201626248del GRCh38
NC_000002.11:g.202490965_202490971del , CM000664.1:g.202490965_202490971del GRCh37
NC_000002.10:g.202199210_202199216del NCBI36
NG_032049.1:g.22282_22288del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471318.6:n.834-101_834-95del
ENST00000621467.5:c.912-101_912-95del ENSP00000480508.2:n.912-101_912-95del
ENST00000686475.1:n.978-101_978-95del
ENST00000409883.7:c.1038-101_1038-95del MANE Select ENSP00000386264.2:n.1038-101_1038-95del
ENST00000286196.9:c.*602-101_*602-95del ENSP00000286196.5:n.*602-101_*602-95del
ENST00000409444.6:c.1014-101_1014-95del ENSP00000387203.2:n.1014-101_1014-95del
ENST00000409883.6:c.1038-101_1038-95del ENSP00000386264.2:n.1038-101_1038-95del
ENST00000471318.5:n.266-101_266-95del
ENST00000495329.1:n.76_82del
ENST00000621467.4:c.1014-101_1014-95del ENSP00000480508.1:n.1014-101_1014-95del
NM_001044385.2:c.1038-101_1038-95del NP_001037850.1:n.1038-101_1038-95del
NM_152388.3:c.1014-101_1014-95del NP_689601.2:n.1014-101_1014-95del
NM_001044385.3:c.1038-101_1038-95del MANE Select NP_001037850.1:n.1038-101_1038-95del
NM_152388.4:c.1014-101_1014-95del NP_689601.2:n.1014-101_1014-95del
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