Canonical Allele Identifier: CA1321143664

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623436_201623437delinsAT , CM000664.2:g.201623436_201623437delinsAT	GRCh38
NC_000002.11:g.202488159_202488160delinsAT , CM000664.1:g.202488159_202488160delinsAT	GRCh37
NC_000002.10:g.202196404_202196405delinsAT	NCBI36
NG_032049.1:g.25093_25094delinsAT
NG_051007.1:g.746_747delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*818_*819delinsAT	ENSP00000480508.2:n.*818_*819delinsAT
ENST00000686475.1:n.1985_1986delinsAT
ENST00000409883.7:c.*818_*819delinsAT MANE Select	ENSP00000386264.2:n.*818_*819delinsAT
ENST00000409444.6:c.*818_*819delinsAT	ENSP00000387203.2:n.*818_*819delinsAT
ENST00000409883.6:c.*818_*819delinsAT	ENSP00000386264.2:n.*818_*819delinsAT
ENST00000495329.1:n.1184_1185delinsAT
NM_001044385.2:c.*818_*819delinsAT	NP_001037850.1:n.*818_*819delinsAT
NM_152388.3:c.*818_*819delinsAT	NP_689601.2:n.*818_*819delinsAT
NM_001044385.3:c.*818_*819delinsAT MANE Select	NP_001037850.1:n.*818_*819delinsAT
NM_152388.4:c.*818_*819delinsAT	NP_689601.2:n.*818_*819delinsAT