Canonical Allele Identifier: CA348231823

Gene: TMEM87B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112067009C>G , CM000664.2:g.112067009C>G	GRCh38
NC_000002.11:g.112824586C>G , CM000664.1:g.112824586C>G	GRCh37
NC_000002.10:g.112541057C>G	NCBI36
NG_051358.1:g.16787C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032824.3:c.392C>G MANE Select	NP_116213.1:p.Thr131Arg
ENST00000283206.9:c.392C>G MANE Select	ENSP00000283206.4:p.Thr131Arg
NM_001329914.1:c.392C>G	NP_001316843.1:p.Thr131Arg
NM_001329914.2:c.392C>G	NP_001316843.1:p.Thr131Arg
NM_032824.2:c.392C>G	NP_116213.1:p.Thr131Arg
ENST00000283206.8:c.392C>G	ENSP00000283206.4:p.Thr131Arg
ENST00000452029.1:c.264C>G
ENST00000452614.5:c.264C>G
ENST00000452614.6:c.392C>G	ENSP00000393998.2:p.Thr131Arg
ENST00000650799.1:c.367C>G
ENST00000650799.2:c.392C>G	ENSP00000498298.2:p.Thr131Arg
XM_005263827.1:c.392C>G	XP_005263884.1:p.Thr131Arg
XM_005263827.2:c.392C>G	XP_005263884.1:p.Thr131Arg
XM_006712807.1:c.392C>G	XP_006712870.1:p.Thr131Arg
XM_017005121.1:c.-70C>G	XP_016860610.1:n.-70C>G
XR_923049.1:n.718C>G
XR_923049.2:n.715C>G