Canonical Allele Identifier: CA2701421127

Gene: TMEM237

Linked Data

• dbSNP Id: rs2105897339

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626087_201626088insC , CM000664.2:g.201626087_201626088insC	GRCh38
NC_000002.11:g.202490810_202490811insC , CM000664.1:g.202490810_202490811insC	GRCh37
NC_000002.10:g.202199055_202199056insC	NCBI36
NG_032049.1:g.22442_22443insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.893_894insG
ENST00000621467.5:c.971_972insG	ENSP00000480508.2:p.Leu325SerfsTer13
ENST00000686475.1:n.1037_1038insG
ENST00000409883.7:c.1097_1098insG MANE Select	ENSP00000386264.2:p.Leu367SerfsTer13
ENST00000286196.9:c.*661_*662insG	ENSP00000286196.5:n.*661_*662insG
ENST00000409444.6:c.1073_1074insG	ENSP00000387203.2:p.Leu359SerfsTer13
ENST00000409883.6:c.1097_1098insG	ENSP00000386264.2:p.Leu367SerfsTer13
ENST00000471318.5:n.325_326insG
ENST00000495329.1:n.236_237insG
ENST00000621467.4:c.1073_1074insG	ENSP00000480508.1:p.Leu359SerfsTer13
NM_001044385.2:c.1097_1098insG	NP_001037850.1:p.Leu367SerfsTer13
NM_152388.3:c.1073_1074insG	NP_689601.2:p.Leu359SerfsTer13
NM_001044385.3:c.1097_1098insG MANE Select	NP_001037850.1:p.Leu367SerfsTer13
NM_152388.4:c.1073_1074insG	NP_689601.2:p.Leu359SerfsTer13