Canonical Allele Identifier: CA1321145674

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625875_201625876delinsAC , CM000664.2:g.201625875_201625876delinsAC	GRCh38
NC_000002.11:g.202490598_202490599delinsAC , CM000664.1:g.202490598_202490599delinsAC	GRCh37
NC_000002.10:g.202198843_202198844delinsAC	NCBI36
NG_032049.1:g.22654_22655delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+150_955+151delinsGT
ENST00000621467.5:c.1033+150_1033+151delinsGT	ENSP00000480508.2:n.1033+150_1033+151delinsGT
ENST00000686475.1:n.1099+150_1099+151delinsGT
ENST00000409883.7:c.1159+150_1159+151delinsGT MANE Select	ENSP00000386264.2:n.1159+150_1159+151delinsGT
ENST00000286196.9:c.*723+150_*723+151delinsGT	ENSP00000286196.5:n.*723+150_*723+151delinsGT
ENST00000409444.6:c.1135+150_1135+151delinsGT	ENSP00000387203.2:n.1135+150_1135+151delinsGT
ENST00000409883.6:c.1159+150_1159+151delinsGT	ENSP00000386264.2:n.1159+150_1159+151delinsGT
ENST00000471318.5:n.387+150_387+151delinsGT
ENST00000495329.1:n.298+150_298+151delinsGT
ENST00000621467.4:c.1135+150_1135+151delinsGT	ENSP00000480508.1:n.1135+150_1135+151delinsGT
NM_001044385.2:c.1159+150_1159+151delinsGT	NP_001037850.1:n.1159+150_1159+151delinsGT
NM_152388.3:c.1135+150_1135+151delinsGT	NP_689601.2:n.1135+150_1135+151delinsGT
NM_001044385.3:c.1159+150_1159+151delinsGT MANE Select	NP_001037850.1:n.1159+150_1159+151delinsGT
NM_152388.4:c.1135+150_1135+151delinsGT	NP_689601.2:n.1135+150_1135+151delinsGT