Canonical Allele Identifier: CA1321145757
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201625981T= , CM000664.2:g.201625981T= GRCh38
NC_000002.11:g.202490704T= , CM000664.1:g.202490704T= GRCh37
NC_000002.10:g.202198949T= NCBI36
NG_032049.1:g.22549A=

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.955+45A=
ENST00000621467.5:c.1033+45A= ENSP00000480508.2:n.1033+45A=
ENST00000686475.1:n.1099+45A=
ENST00000409883.7:c.1159+45A= MANE Select ENSP00000386264.2:n.1159+45A=
ENST00000286196.9:c.*723+45A= ENSP00000286196.5:n.*723+45A=
ENST00000409444.6:c.1135+45A= ENSP00000387203.2:n.1135+45A=
ENST00000409883.6:c.1159+45A= ENSP00000386264.2:n.1159+45A=
ENST00000471318.5:n.387+45A=
ENST00000495329.1:n.298+45A=
ENST00000621467.4:c.1135+45A= ENSP00000480508.1:n.1135+45A=
NM_001044385.2:c.1159+45A= NP_001037850.1:n.1159+45A=
NM_152388.3:c.1135+45A= NP_689601.2:n.1135+45A=
NM_001044385.3:c.1159+45A= MANE Select NP_001037850.1:n.1159+45A=
NM_152388.4:c.1135+45A= NP_689601.2:n.1135+45A=