Canonical Allele Identifier: CA430663968

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490768T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626045T>G , CM000664.2:g.201626045T>G	GRCh38
NC_000002.11:g.202490768T>G , CM000664.1:g.202490768T>G	GRCh37
NC_000002.10:g.202199013T>G	NCBI36
NG_032049.1:g.22485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.936A>C
ENST00000621467.5:c.1014A>C	ENSP00000480508.2:p.Pro338=
ENST00000686475.1:n.1080A>C
ENST00000409883.7:c.1140A>C MANE Select	ENSP00000386264.2:p.Pro380=
ENST00000286196.9:c.*704A>C	ENSP00000286196.5:n.*704A>C
ENST00000409444.6:c.1116A>C	ENSP00000387203.2:p.Pro372=
ENST00000409883.6:c.1140A>C	ENSP00000386264.2:p.Pro380=
ENST00000471318.5:n.368A>C
ENST00000495329.1:n.279A>C
ENST00000621467.4:c.1116A>C	ENSP00000480508.1:p.Pro372=
NM_001044385.2:c.1140A>C	NP_001037850.1:p.Pro380=
NM_152388.3:c.1116A>C	NP_689601.2:p.Pro372=
NM_001044385.3:c.1140A>C MANE Select	NP_001037850.1:p.Pro380=
NM_152388.4:c.1116A>C	NP_689601.2:p.Pro372=