Canonical Allele Identifier: CA350304674
Gene: TMEM237 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626113A>C , CM000664.2:g.201626113A>C GRCh38
NC_000002.11:g.202490836A>C , CM000664.1:g.202490836A>C GRCh37
NC_000002.10:g.202199081A>C NCBI36
NG_032049.1:g.22417T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000471318.6:n.868T>G
ENST00000621467.5:c.946T>G ENSP00000480508.2:p.Trp316Gly
ENST00000686475.1:n.1012T>G
ENST00000409883.7:c.1072T>G MANE Select ENSP00000386264.2:p.Trp358Gly
ENST00000286196.9:c.*636T>G ENSP00000286196.5:n.*636T>G
ENST00000409444.6:c.1048T>G ENSP00000387203.2:p.Trp350Gly
ENST00000409883.6:c.1072T>G ENSP00000386264.2:p.Trp358Gly
ENST00000471318.5:n.300T>G
ENST00000495329.1:n.211T>G
ENST00000621467.4:c.1048T>G ENSP00000480508.1:p.Trp350Gly
NM_001044385.2:c.1072T>G NP_001037850.1:p.Trp358Gly
NM_152388.3:c.1048T>G NP_689601.2:p.Trp350Gly
NM_001044385.3:c.1072T>G MANE Select NP_001037850.1:p.Trp358Gly
NM_152388.4:c.1048T>G NP_689601.2:p.Trp350Gly