Canonical Allele Identifier: CA350314365
Community Standard Title: NM_001044385.3(TMEM237):c.278T>A (p.Leu93Ter)
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201633428A>T , CM000664.2:g.201633428A>T GRCh38
NC_000002.11:g.202498151A>T , CM000664.1:g.202498151A>T GRCh37
NC_000002.10:g.202206396A>T NCBI36
NG_032049.1:g.15102T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001044385.3:c.278T>A MANE Select NP_001037850.1:p.Leu93Ter
ENST00000409883.7:c.278T>A MANE Select ENSP00000386264.2:p.Leu93Ter
NM_001044385.2:c.278T>A NP_001037850.1:p.Leu93Ter
NM_152388.3:c.254T>A NP_689601.2:p.Leu85Ter
NM_152388.4:c.254T>A NP_689601.2:p.Leu85Ter
ENST00000286196.9:c.199T>A ENSP00000286196.5:p.Trp67Arg
ENST00000409444.6:c.254T>A ENSP00000387203.2:p.Leu85Ter
ENST00000409883.6:c.278T>A ENSP00000386264.2:p.Leu93Ter
ENST00000432684.6:c.*77T>A ENSP00000413230.2:n.*77T>A
ENST00000444047.6:c.*88T>A ENSP00000402681.2:n.*88T>A
ENST00000471318.6:n.168T>A
ENST00000489550.5:n.381T>A
ENST00000621467.4:c.254T>A ENSP00000480508.1:p.Leu85Ter
ENST00000621467.5:c.152T>A ENSP00000480508.2:p.Leu51Ter
ENST00000686475.1:n.114T>A