Canonical Allele Identifier: CA439533719

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396327G>A , CM000666.2:g.55396327G>A	GRCh38
NC_000004.11:g.56262494G>A , CM000666.1:g.56262494G>A	GRCh37
NC_000004.10:g.55957251G>A	NCBI36
NG_032881.1:g.5415G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.138G>A MANE Select	NP_060945.2:p.Pro46=
ENST00000381334.10:c.138G>A MANE Select	ENSP00000370736.5:p.Pro46=
NM_018475.4:c.138G>A	NP_060945.2:p.Pro46=
NR_073070.1:n.415G>A
NR_073070.2:n.371G>A
ENST00000381334.9:c.138G>A	ENSP00000370736.5:p.Pro46=
ENST00000506198.5:c.138G>A	ENSP00000425449.1:p.Pro46=
ENST00000508404.5:c.138G>A	ENSP00000422639.1:p.Pro46=
ENST00000514070.1:n.77G>A
XM_011534394.1:c.138G>A	XP_011532696.1:p.Pro46=
XM_011534394.3:c.138G>A	XP_011532696.1:p.Pro46=
XM_017008412.1:c.-308G>A	XP_016863901.1:n.-308G>A
XR_001741287.2:n.675G>A