Canonical Allele Identifier: CA350304281
Gene: TMEM237 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626052T>G , CM000664.2:g.201626052T>G GRCh38
NC_000002.11:g.202490775T>G , CM000664.1:g.202490775T>G GRCh37
NC_000002.10:g.202199020T>G NCBI36
NG_032049.1:g.22478A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.929A>C
ENST00000621467.5:c.1007A>C ENSP00000480508.2:p.Tyr336Ser
ENST00000686475.1:n.1073A>C
ENST00000409883.7:c.1133A>C MANE Select ENSP00000386264.2:p.Tyr378Ser
ENST00000286196.9:c.*697A>C ENSP00000286196.5:n.*697A>C
ENST00000409444.6:c.1109A>C ENSP00000387203.2:p.Tyr370Ser
ENST00000409883.6:c.1133A>C ENSP00000386264.2:p.Tyr378Ser
ENST00000471318.5:n.361A>C
ENST00000495329.1:n.272A>C
ENST00000621467.4:c.1109A>C ENSP00000480508.1:p.Tyr370Ser
NM_001044385.2:c.1133A>C NP_001037850.1:p.Tyr378Ser
NM_152388.3:c.1109A>C NP_689601.2:p.Tyr370Ser
NM_001044385.3:c.1133A>C MANE Select NP_001037850.1:p.Tyr378Ser
NM_152388.4:c.1109A>C NP_689601.2:p.Tyr370Ser