Canonical Allele Identifier: CA430664104

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490788G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626065G>A , CM000664.2:g.201626065G>A	GRCh38
NC_000002.11:g.202490788G>A , CM000664.1:g.202490788G>A	GRCh37
NC_000002.10:g.202199033G>A	NCBI36
NG_032049.1:g.22465C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000471318.6:n.916C>T
ENST00000621467.5:c.994C>T	ENSP00000480508.2:p.Leu332=
ENST00000686475.1:n.1060C>T
ENST00000409883.7:c.1120C>T MANE Select	ENSP00000386264.2:p.Leu374=
ENST00000286196.9:c.*684C>T	ENSP00000286196.5:n.*684C>T
ENST00000409444.6:c.1096C>T	ENSP00000387203.2:p.Leu366=
ENST00000409883.6:c.1120C>T	ENSP00000386264.2:p.Leu374=
ENST00000471318.5:n.348C>T
ENST00000495329.1:n.259C>T
ENST00000621467.4:c.1096C>T	ENSP00000480508.1:p.Leu366=
NM_001044385.2:c.1120C>T	NP_001037850.1:p.Leu374=
NM_152388.3:c.1096C>T	NP_689601.2:p.Leu366=
NM_001044385.3:c.1120C>T MANE Select	NP_001037850.1:p.Leu374=
NM_152388.4:c.1096C>T	NP_689601.2:p.Leu366=