Canonical Allele Identifier: CA2753880997
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621211del , CM000664.2:g.201621211del GRCh38
NC_000002.11:g.202485934del , CM000664.1:g.202485934del GRCh37
NC_000002.10:g.202194179del NCBI36
NG_032049.1:g.27319del
NG_051007.1:g.2972del

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*3044del ENSP00000480508.2:n.*3044del
ENST00000686475.1:n.4211del
ENST00000409883.7:c.*3044del MANE Select ENSP00000386264.2:n.*3044del
ENST00000409444.6:c.*3044del ENSP00000387203.2:n.*3044del
ENST00000409883.6:c.*3044del ENSP00000386264.2:n.*3044del
ENST00000495329.1:n.3410del
NM_001044385.2:c.*3044del NP_001037850.1:n.*3044del
NM_152388.3:c.*3044del NP_689601.2:n.*3044del
NM_001044385.3:c.*3044del MANE Select NP_001037850.1:n.*3044del
NM_152388.4:c.*3044del NP_689601.2:n.*3044del