Canonical Allele Identifier: CA2753880764

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623469_201623470insAAAAAAAAAA , CM000664.2:g.201623469_201623470insAAAAAAAAAA	GRCh38
NC_000002.11:g.202488192_202488193insAAAAAAAAAA , CM000664.1:g.202488192_202488193insAAAAAAAAAA	GRCh37
NC_000002.10:g.202196437_202196438insAAAAAAAAAA	NCBI36
NG_032049.1:g.25066_25067insTTTTTTTTTT
NG_051007.1:g.719_720insTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*791_*792insTTTTTTTTTT	ENSP00000480508.2:n.*791_*792insTTTTTTTTTT
ENST00000686475.1:n.1958_1959insTTTTTTTTTT
ENST00000409883.7:c.*791_*792insTTTTTTTTTT MANE Select	ENSP00000386264.2:n.*791_*792insTTTTTTTTTT
ENST00000409444.6:c.*791_*792insTTTTTTTTTT	ENSP00000387203.2:n.*791_*792insTTTTTTTTTT
ENST00000409883.6:c.*791_*792insTTTTTTTTTT	ENSP00000386264.2:n.*791_*792insTTTTTTTTTT
ENST00000495329.1:n.1157_1158insTTTTTTTTTT
NM_001044385.2:c.*791_*792insTTTTTTTTTT	NP_001037850.1:n.*791_*792insTTTTTTTTTT
NM_152388.3:c.*791_*792insTTTTTTTTTT	NP_689601.2:n.*791_*792insTTTTTTTTTT
NM_001044385.3:c.*791_*792insTTTTTTTTTT MANE Select	NP_001037850.1:n.*791_*792insTTTTTTTTTT
NM_152388.4:c.*791_*792insTTTTTTTTTT	NP_689601.2:n.*791_*792insTTTTTTTTTT