Canonical Allele Identifier: CA350316567

Gene: TMEM237

Linked Data

• MyVariant Identifiers: chr2:g.202504988A>T (hg19) ; chr2:g.201640265A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640265A>T , CM000664.2:g.201640265A>T	GRCh38
NC_000002.11:g.202504988A>T , CM000664.1:g.202504988A>T	GRCh37
NC_000002.10:g.202213233A>T	NCBI36
NG_032049.1:g.8265T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+628T>A	ENSP00000480508.2:n.-356+628T>A
ENST00000409883.7:c.75T>A MANE Select	ENSP00000386264.2:p.Ser25Arg
ENST00000286196.9:c.-1+628T>A	ENSP00000286196.5:n.-1+628T>A
ENST00000409444.6:c.51T>A	ENSP00000387203.2:p.Ser17Arg
ENST00000409883.6:c.75T>A	ENSP00000386264.2:p.Ser25Arg
ENST00000432684.6:c.75T>A	ENSP00000413230.2:p.Ser25Arg
ENST00000444047.6:c.75T>A	ENSP00000402681.2:p.Ser25Arg
ENST00000463205.2:n.78T>A
ENST00000489550.5:n.92+628T>A
ENST00000621467.4:c.50+628T>A	ENSP00000480508.1:n.50+628T>A
NM_001044385.2:c.75T>A	NP_001037850.1:p.Ser25Arg
NM_152388.3:c.51T>A	NP_689601.2:p.Ser17Arg
NM_001044385.3:c.75T>A MANE Select	NP_001037850.1:p.Ser25Arg
NM_152388.4:c.51T>A	NP_689601.2:p.Ser17Arg