Canonical Allele Identifier: CA1321145745

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625963_201625964delinsAG , CM000664.2:g.201625963_201625964delinsAG	GRCh38
NC_000002.11:g.202490686_202490687delinsAG , CM000664.1:g.202490686_202490687delinsAG	GRCh37
NC_000002.10:g.202198931_202198932delinsAG	NCBI36
NG_032049.1:g.22566_22567delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+62_955+63delinsCT
ENST00000621467.5:c.1033+62_1033+63delinsCT	ENSP00000480508.2:n.1033+62_1033+63delinsCT
ENST00000686475.1:n.1099+62_1099+63delinsCT
ENST00000409883.7:c.1159+62_1159+63delinsCT MANE Select	ENSP00000386264.2:n.1159+62_1159+63delinsCT
ENST00000286196.9:c.*723+62_*723+63delinsCT	ENSP00000286196.5:n.*723+62_*723+63delinsCT
ENST00000409444.6:c.1135+62_1135+63delinsCT	ENSP00000387203.2:n.1135+62_1135+63delinsCT
ENST00000409883.6:c.1159+62_1159+63delinsCT	ENSP00000386264.2:n.1159+62_1159+63delinsCT
ENST00000471318.5:n.387+62_387+63delinsCT
ENST00000495329.1:n.298+62_298+63delinsCT
ENST00000621467.4:c.1135+62_1135+63delinsCT	ENSP00000480508.1:n.1135+62_1135+63delinsCT
NM_001044385.2:c.1159+62_1159+63delinsCT	NP_001037850.1:n.1159+62_1159+63delinsCT
NM_152388.3:c.1135+62_1135+63delinsCT	NP_689601.2:n.1135+62_1135+63delinsCT
NM_001044385.3:c.1159+62_1159+63delinsCT MANE Select	NP_001037850.1:n.1159+62_1159+63delinsCT
NM_152388.4:c.1135+62_1135+63delinsCT	NP_689601.2:n.1135+62_1135+63delinsCT