Canonical Allele Identifier: CA2925579

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55417974G>A , CM000666.2:g.55417974G>A	GRCh38
NC_000004.11:g.56284141G>A , CM000666.1:g.56284141G>A	GRCh37
NC_000004.10:g.55978898G>A	NCBI36
NG_032881.1:g.27062G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.781G>A MANE Select	NP_060945.2:p.Ala261Thr
ENST00000381334.10:c.781G>A MANE Select	ENSP00000370736.5:p.Ala261Thr
NM_018475.4:c.781G>A	NP_060945.2:p.Ala261Thr
NR_073070.1:n.1161G>A
NR_073070.2:n.1117G>A
ENST00000381334.9:c.781G>A	ENSP00000370736.5:p.Ala261Thr
ENST00000506103.2:c.56G>A
ENST00000506198.5:c.208-6564G>A	ENSP00000425449.1:n.208-6564G>A
ENST00000508404.5:c.*653G>A	ENSP00000422639.1:n.*653G>A
ENST00000508561.5:n.372-74G>A
ENST00000509575.1:n.284G>A
ENST00000514904.5:n.1235G>A
ENST00000608091.1:c.291G>A
XM_011534394.1:c.781G>A	XP_011532696.1:p.Ala261Thr
XM_011534394.3:c.781G>A	XP_011532696.1:p.Ala261Thr
XM_017008412.1:c.592G>A	XP_016863901.1:p.Ala198Thr
XR_001741287.2:n.1318G>A