Canonical Allele Identifier: CA2577211812

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625997A>G , CM000664.2:g.201625997A>G	GRCh38
NC_000002.11:g.202490720A>G , CM000664.1:g.202490720A>G	GRCh37
NC_000002.10:g.202198965A>G	NCBI36
NG_032049.1:g.22533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+29T>C
ENST00000621467.5:c.1033+29T>C	ENSP00000480508.2:n.1033+29T>C
ENST00000686475.1:n.1099+29T>C
ENST00000409883.7:c.1159+29T>C MANE Select	ENSP00000386264.2:n.1159+29T>C
ENST00000286196.9:c.*723+29T>C	ENSP00000286196.5:n.*723+29T>C
ENST00000409444.6:c.1135+29T>C	ENSP00000387203.2:n.1135+29T>C
ENST00000409883.6:c.1159+29T>C	ENSP00000386264.2:n.1159+29T>C
ENST00000471318.5:n.387+29T>C
ENST00000495329.1:n.298+29T>C
ENST00000621467.4:c.1135+29T>C	ENSP00000480508.1:n.1135+29T>C
NM_001044385.2:c.1159+29T>C	NP_001037850.1:n.1159+29T>C
NM_152388.3:c.1135+29T>C	NP_689601.2:n.1135+29T>C
NM_001044385.3:c.1159+29T>C MANE Select	NP_001037850.1:n.1159+29T>C
NM_152388.4:c.1135+29T>C	NP_689601.2:n.1135+29T>C