Canonical Allele Identifier: CA2662657686

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626367-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626367_201626368insG , CM000664.2:g.201626367_201626368insG	GRCh38
NC_000002.11:g.202491090_202491091insG , CM000664.1:g.202491090_202491091insG	GRCh37
NC_000002.10:g.202199335_202199336insG	NCBI36
NG_032049.1:g.22162_22163insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-221_834-220insC
ENST00000621467.5:c.912-221_912-220insC	ENSP00000480508.2:n.912-221_912-220insC
ENST00000686475.1:n.978-221_978-220insC
ENST00000409883.7:c.1038-221_1038-220insC MANE Select	ENSP00000386264.2:n.1038-221_1038-220insC
ENST00000286196.9:c.*602-221_*602-220insC	ENSP00000286196.5:n.*602-221_*602-220insC
ENST00000409444.6:c.1014-221_1014-220insC	ENSP00000387203.2:n.1014-221_1014-220insC
ENST00000409883.6:c.1038-221_1038-220insC	ENSP00000386264.2:n.1038-221_1038-220insC
ENST00000471318.5:n.266-221_266-220insC
ENST00000621467.4:c.1014-221_1014-220insC	ENSP00000480508.1:n.1014-221_1014-220insC
NM_001044385.2:c.1038-221_1038-220insC	NP_001037850.1:n.1038-221_1038-220insC
NM_152388.3:c.1014-221_1014-220insC	NP_689601.2:n.1014-221_1014-220insC
NM_001044385.3:c.1038-221_1038-220insC MANE Select	NP_001037850.1:n.1038-221_1038-220insC
NM_152388.4:c.1014-221_1014-220insC	NP_689601.2:n.1014-221_1014-220insC