Canonical Allele Identifier: CA350304589

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202490823T>G (hg19) ; chr2:g.201626100T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626100T>G , CM000664.2:g.201626100T>G	GRCh38
NC_000002.11:g.202490823T>G , CM000664.1:g.202490823T>G	GRCh37
NC_000002.10:g.202199068T>G	NCBI36
NG_032049.1:g.22430A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.881A>C
ENST00000621467.5:c.959A>C	ENSP00000480508.2:p.Asn320Thr
ENST00000686475.1:n.1025A>C
ENST00000409883.7:c.1085A>C MANE Select	ENSP00000386264.2:p.Asn362Thr
ENST00000286196.9:c.*649A>C	ENSP00000286196.5:n.*649A>C
ENST00000409444.6:c.1061A>C	ENSP00000387203.2:p.Asn354Thr
ENST00000409883.6:c.1085A>C	ENSP00000386264.2:p.Asn362Thr
ENST00000471318.5:n.313A>C
ENST00000495329.1:n.224A>C
ENST00000621467.4:c.1061A>C	ENSP00000480508.1:p.Asn354Thr
NM_001044385.2:c.1085A>C	NP_001037850.1:p.Asn362Thr
NM_152388.3:c.1061A>C	NP_689601.2:p.Asn354Thr
NM_001044385.3:c.1085A>C MANE Select	NP_001037850.1:p.Asn362Thr
NM_152388.4:c.1061A>C	NP_689601.2:p.Asn354Thr