Canonical Allele Identifier: CA2662657501

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201625881-CTTTAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625885_201625889del , CM000664.2:g.201625885_201625889del	GRCh38
NC_000002.11:g.202490608_202490612del , CM000664.1:g.202490608_202490612del	GRCh37
NC_000002.10:g.202198853_202198857del	NCBI36
NG_032049.1:g.22644_22648del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.955+140_955+144del
ENST00000621467.5:c.1033+140_1033+144del	ENSP00000480508.2:n.1033+140_1033+144del
ENST00000686475.1:n.1099+140_1099+144del
ENST00000409883.7:c.1159+140_1159+144del MANE Select	ENSP00000386264.2:n.1159+140_1159+144del
ENST00000286196.9:c.*723+140_*723+144del	ENSP00000286196.5:n.*723+140_*723+144del
ENST00000409444.6:c.1135+140_1135+144del	ENSP00000387203.2:n.1135+140_1135+144del
ENST00000409883.6:c.1159+140_1159+144del	ENSP00000386264.2:n.1159+140_1159+144del
ENST00000471318.5:n.387+140_387+144del
ENST00000495329.1:n.298+140_298+144del
ENST00000621467.4:c.1135+140_1135+144del	ENSP00000480508.1:n.1135+140_1135+144del
NM_001044385.2:c.1159+140_1159+144del	NP_001037850.1:n.1159+140_1159+144del
NM_152388.3:c.1135+140_1135+144del	NP_689601.2:n.1135+140_1135+144del
NM_001044385.3:c.1159+140_1159+144del MANE Select	NP_001037850.1:n.1159+140_1159+144del
NM_152388.4:c.1135+140_1135+144del	NP_689601.2:n.1135+140_1135+144del