Canonical Allele Identifier: CA1321145580

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625775_201625776delinsAC , CM000664.2:g.201625775_201625776delinsAC	GRCh38
NC_000002.11:g.202490498_202490499delinsAC , CM000664.1:g.202490498_202490499delinsAC	GRCh37
NC_000002.10:g.202198743_202198744delinsAC	NCBI36
NG_032049.1:g.22754_22755delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+250_955+251delinsGT
ENST00000621467.5:c.1033+250_1033+251delinsGT	ENSP00000480508.2:n.1033+250_1033+251delinsGT
ENST00000686475.1:n.1099+250_1099+251delinsGT
ENST00000409883.7:c.1159+250_1159+251delinsGT MANE Select	ENSP00000386264.2:n.1159+250_1159+251delinsGT
ENST00000286196.9:c.*723+250_*723+251delinsGT	ENSP00000286196.5:n.*723+250_*723+251delinsGT
ENST00000409444.6:c.1135+250_1135+251delinsGT	ENSP00000387203.2:n.1135+250_1135+251delinsGT
ENST00000409883.6:c.1159+250_1159+251delinsGT	ENSP00000386264.2:n.1159+250_1159+251delinsGT
ENST00000471318.5:n.387+250_387+251delinsGT
ENST00000495329.1:n.298+250_298+251delinsGT
ENST00000621467.4:c.1135+250_1135+251delinsGT	ENSP00000480508.1:n.1135+250_1135+251delinsGT
NM_001044385.2:c.1159+250_1159+251delinsGT	NP_001037850.1:n.1159+250_1159+251delinsGT
NM_152388.3:c.1135+250_1135+251delinsGT	NP_689601.2:n.1135+250_1135+251delinsGT
NM_001044385.3:c.1159+250_1159+251delinsGT MANE Select	NP_001037850.1:n.1159+250_1159+251delinsGT
NM_152388.4:c.1135+250_1135+251delinsGT	NP_689601.2:n.1135+250_1135+251delinsGT