Canonical Allele Identifier: CA1321145549

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625715_201625717delinsAAG , CM000664.2:g.201625715_201625717delinsAAG	GRCh38
NC_000002.11:g.202490438_202490440delinsAAG , CM000664.1:g.202490438_202490440delinsAAG	GRCh37
NC_000002.10:g.202198683_202198685delinsAAG	NCBI36
NG_032049.1:g.22813_22815delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+309_955+311delinsCTT
ENST00000621467.5:c.1033+309_1033+311delinsCTT	ENSP00000480508.2:n.1033+309_1033+311delinsCTT
ENST00000686475.1:n.1099+309_1099+311delinsCTT
ENST00000409883.7:c.1159+309_1159+311delinsCTT MANE Select	ENSP00000386264.2:n.1159+309_1159+311delinsCTT
ENST00000286196.9:c.*723+309_*723+311delinsCTT	ENSP00000286196.5:n.*723+309_*723+311delinsCTT
ENST00000409444.6:c.1135+309_1135+311delinsCTT	ENSP00000387203.2:n.1135+309_1135+311delinsCTT
ENST00000409883.6:c.1159+309_1159+311delinsCTT	ENSP00000386264.2:n.1159+309_1159+311delinsCTT
ENST00000471318.5:n.387+309_387+311delinsCTT
ENST00000495329.1:n.298+309_298+311delinsCTT
ENST00000621467.4:c.1135+309_1135+311delinsCTT	ENSP00000480508.1:n.1135+309_1135+311delinsCTT
NM_001044385.2:c.1159+309_1159+311delinsCTT	NP_001037850.1:n.1159+309_1159+311delinsCTT
NM_152388.3:c.1135+309_1135+311delinsCTT	NP_689601.2:n.1135+309_1135+311delinsCTT
NM_001044385.3:c.1159+309_1159+311delinsCTT MANE Select	NP_001037850.1:n.1159+309_1159+311delinsCTT
NM_152388.4:c.1135+309_1135+311delinsCTT	NP_689601.2:n.1135+309_1135+311delinsCTT