Canonical Allele Identifier: CA2753880979

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201621201T>C , CM000664.2:g.201621201T>C	GRCh38
NC_000002.11:g.202485924T>C , CM000664.1:g.202485924T>C	GRCh37
NC_000002.10:g.202194169T>C	NCBI36
NG_032049.1:g.27329A>G
NG_051007.1:g.2982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*3054A>G	ENSP00000480508.2:n.*3054A>G
ENST00000686475.1:n.4221A>G
ENST00000409883.7:c.*3054A>G MANE Select	ENSP00000386264.2:n.*3054A>G
ENST00000409444.6:c.*3054A>G	ENSP00000387203.2:n.*3054A>G
ENST00000409883.6:c.*3054A>G	ENSP00000386264.2:n.*3054A>G
ENST00000495329.1:n.3420A>G
NM_001044385.2:c.*3054A>G	NP_001037850.1:n.*3054A>G
NM_152388.3:c.*3054A>G	NP_689601.2:n.*3054A>G
NM_001044385.3:c.*3054A>G MANE Select	NP_001037850.1:n.*3054A>G
NM_152388.4:c.*3054A>G	NP_689601.2:n.*3054A>G