Canonical Allele Identifier: CA2056293
Gene: TMEM237 HGNC NCBI

Linked Data

dbSNP Id: rs748301153

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626034A>G , CM000664.2:g.201626034A>G GRCh38
NC_000002.11:g.202490757A>G , CM000664.1:g.202490757A>G GRCh37
NC_000002.10:g.202199002A>G NCBI36
NG_032049.1:g.22496T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000471318.6:n.947T>C
ENST00000621467.5:c.1025T>C ENSP00000480508.2:p.Leu342Pro
ENST00000686475.1:n.1091T>C
ENST00000409883.7:c.1151T>C MANE Select ENSP00000386264.2:p.Leu384Pro
ENST00000286196.9:c.*715T>C ENSP00000286196.5:n.*715T>C
ENST00000409444.6:c.1127T>C ENSP00000387203.2:p.Leu376Pro
ENST00000409883.6:c.1151T>C ENSP00000386264.2:p.Leu384Pro
ENST00000471318.5:n.379T>C
ENST00000495329.1:n.290T>C
ENST00000621467.4:c.1127T>C ENSP00000480508.1:p.Leu376Pro
NM_001044385.2:c.1151T>C NP_001037850.1:p.Leu384Pro
NM_152388.3:c.1127T>C NP_689601.2:p.Leu376Pro
NM_001044385.3:c.1151T>C MANE Select NP_001037850.1:p.Leu384Pro
NM_152388.4:c.1127T>C NP_689601.2:p.Leu376Pro