Canonical Allele Identifier: CA2056574

Gene: TMEM237

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201638988C>A , CM000664.2:g.201638988C>A	GRCh38
NC_000002.11:g.202503711C>A , CM000664.1:g.202503711C>A	GRCh37
NC_000002.10:g.202211956C>A	NCBI36
NG_032049.1:g.9542G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001044385.3:c.136+1G>T MANE Select	NP_001037850.1:n.136+1G>T
ENST00000409883.7:c.136+1G>T MANE Select	ENSP00000386264.2:n.136+1G>T
NM_001044385.2:c.136+1G>T	NP_001037850.1:n.136+1G>T
NM_152388.3:c.112+1G>T	NP_689601.2:n.112+1G>T
NM_152388.4:c.112+1G>T	NP_689601.2:n.112+1G>T
ENST00000286196.9:c.57+1G>T	ENSP00000286196.5:n.57+1G>T
ENST00000409444.6:c.112+1G>T	ENSP00000387203.2:n.112+1G>T
ENST00000409883.6:c.136+1G>T	ENSP00000386264.2:n.136+1G>T
ENST00000432684.6:c.136+1G>T	ENSP00000413230.2:n.136+1G>T
ENST00000444047.6:c.136+1G>T	ENSP00000402681.2:n.136+1G>T
ENST00000463205.2:n.140G>T
ENST00000480124.1:n.43+1G>T
ENST00000489550.5:n.149+1G>T
ENST00000621467.4:c.112+1G>T	ENSP00000480508.1:n.112+1G>T
ENST00000621467.5:c.-299+1G>T	ENSP00000480508.2:n.-299+1G>T