Canonical Allele Identifier: CA1041263082

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957752431
• gnomAD v3: 2-201625659-CAG-C
• gnomAD v4: 2-201625659-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625664_201625665del , CM000664.2:g.201625664_201625665del	GRCh38
NC_000002.11:g.202490387_202490388del , CM000664.1:g.202490387_202490388del	GRCh37
NC_000002.10:g.202198632_202198633del	NCBI36
NG_032049.1:g.22869_22870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+365_955+366del
ENST00000621467.5:c.1033+365_1033+366del	ENSP00000480508.2:n.1033+365_1033+366del
ENST00000686475.1:n.1099+365_1099+366del
ENST00000409883.7:c.1159+365_1159+366del MANE Select	ENSP00000386264.2:n.1159+365_1159+366del
ENST00000286196.9:c.*723+365_*723+366del	ENSP00000286196.5:n.*723+365_*723+366del
ENST00000409444.6:c.1135+365_1135+366del	ENSP00000387203.2:n.1135+365_1135+366del
ENST00000409883.6:c.1159+365_1159+366del	ENSP00000386264.2:n.1159+365_1159+366del
ENST00000471318.5:n.387+365_387+366del
ENST00000495329.1:n.298+365_298+366del
ENST00000621467.4:c.1135+365_1135+366del	ENSP00000480508.1:n.1135+365_1135+366del
NM_001044385.2:c.1159+365_1159+366del	NP_001037850.1:n.1159+365_1159+366del
NM_152388.3:c.1135+365_1135+366del	NP_689601.2:n.1135+365_1135+366del
NM_001044385.3:c.1159+365_1159+366del MANE Select	NP_001037850.1:n.1159+365_1159+366del
NM_152388.4:c.1135+365_1135+366del	NP_689601.2:n.1135+365_1135+366del