Canonical Allele Identifier: CA356958976

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396380A>G , CM000666.2:g.55396380A>G	GRCh38
NC_000004.11:g.56262547A>G , CM000666.1:g.56262547A>G	GRCh37
NC_000004.10:g.55957304A>G	NCBI36
NG_032881.1:g.5468A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.191A>G MANE Select	NP_060945.2:p.Glu64Gly
ENST00000381334.10:c.191A>G MANE Select	ENSP00000370736.5:p.Glu64Gly
NM_018475.4:c.191A>G	NP_060945.2:p.Glu64Gly
NR_073070.1:n.468A>G
NR_073070.2:n.424A>G
ENST00000381334.9:c.191A>G	ENSP00000370736.5:p.Glu64Gly
ENST00000506198.5:c.191A>G	ENSP00000425449.1:p.Glu64Gly
ENST00000508404.5:c.191A>G	ENSP00000422639.1:p.Glu64Gly
ENST00000514070.1:n.130A>G
XM_011534394.1:c.191A>G	XP_011532696.1:p.Glu64Gly
XM_011534394.3:c.191A>G	XP_011532696.1:p.Glu64Gly
XM_017008412.1:c.-255A>G	XP_016863901.1:n.-255A>G
XR_001741287.2:n.728A>G