Canonical Allele Identifier: CA1321145693
Gene: TMEM237 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201625897C= , CM000664.2:g.201625897C= GRCh38
NC_000002.11:g.202490620C= , CM000664.1:g.202490620C= GRCh37
NC_000002.10:g.202198865C= NCBI36
NG_032049.1:g.22633G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000471318.6:n.955+129G=
ENST00000621467.5:c.1033+129G= ENSP00000480508.2:n.1033+129G=
ENST00000686475.1:n.1099+129G=
ENST00000409883.7:c.1159+129G= MANE Select ENSP00000386264.2:n.1159+129G=
ENST00000286196.9:c.*723+129G= ENSP00000286196.5:n.*723+129G=
ENST00000409444.6:c.1135+129G= ENSP00000387203.2:n.1135+129G=
ENST00000409883.6:c.1159+129G= ENSP00000386264.2:n.1159+129G=
ENST00000471318.5:n.387+129G=
ENST00000495329.1:n.298+129G=
ENST00000621467.4:c.1135+129G= ENSP00000480508.1:n.1135+129G=
NM_001044385.2:c.1159+129G= NP_001037850.1:n.1159+129G=
NM_152388.3:c.1135+129G= NP_689601.2:n.1135+129G=
NM_001044385.3:c.1159+129G= MANE Select NP_001037850.1:n.1159+129G=
NM_152388.4:c.1135+129G= NP_689601.2:n.1135+129G=