Canonical Allele Identifier: CA1321143757

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623529_201623532delinsCCTT , CM000664.2:g.201623529_201623532delinsCCTT	GRCh38
NC_000002.11:g.202488252_202488255delinsCCTT , CM000664.1:g.202488252_202488255delinsCCTT	GRCh37
NC_000002.10:g.202196497_202196500delinsCCTT	NCBI36
NG_032049.1:g.24998_25001delinsAAGG
NG_051007.1:g.651_654delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*723_*726delinsAAGG	ENSP00000480508.2:n.*723_*726delinsAAGG
ENST00000686475.1:n.1890_1893delinsAAGG
ENST00000409883.7:c.*723_*726delinsAAGG MANE Select	ENSP00000386264.2:n.*723_*726delinsAAGG
ENST00000409444.6:c.*723_*726delinsAAGG	ENSP00000387203.2:n.*723_*726delinsAAGG
ENST00000409883.6:c.*723_*726delinsAAGG	ENSP00000386264.2:n.*723_*726delinsAAGG
ENST00000495329.1:n.1089_1092delinsAAGG
NM_001044385.2:c.*723_*726delinsAAGG	NP_001037850.1:n.*723_*726delinsAAGG
NM_152388.3:c.*723_*726delinsAAGG	NP_689601.2:n.*723_*726delinsAAGG
NM_001044385.3:c.*723_*726delinsAAGG MANE Select	NP_001037850.1:n.*723_*726delinsAAGG
NM_152388.4:c.*723_*726delinsAAGG	NP_689601.2:n.*723_*726delinsAAGG