Canonical Allele Identifier: CA2753880977
Gene: TMEM237 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621200_201621201insA , CM000664.2:g.201621200_201621201insA GRCh38
NC_000002.11:g.202485923_202485924insA , CM000664.1:g.202485923_202485924insA GRCh37
NC_000002.10:g.202194168_202194169insA NCBI36
NG_032049.1:g.27329_27330insT
NG_051007.1:g.2982_2983insT

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3054_*3055insT ENSP00000480508.2:n.*3054_*3055insT
ENST00000686475.1:n.4221_4222insT
ENST00000409883.7:c.*3054_*3055insT MANE Select ENSP00000386264.2:n.*3054_*3055insT
ENST00000409444.6:c.*3054_*3055insT ENSP00000387203.2:n.*3054_*3055insT
ENST00000409883.6:c.*3054_*3055insT ENSP00000386264.2:n.*3054_*3055insT
ENST00000495329.1:n.3420_3421insT
NM_001044385.2:c.*3054_*3055insT NP_001037850.1:n.*3054_*3055insT
NM_152388.3:c.*3054_*3055insT NP_689601.2:n.*3054_*3055insT
NM_001044385.3:c.*3054_*3055insT MANE Select NP_001037850.1:n.*3054_*3055insT
NM_152388.4:c.*3054_*3055insT NP_689601.2:n.*3054_*3055insT
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