Canonical Allele Identifier: CA2925536

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55417165G>A , CM000666.2:g.55417165G>A	GRCh38
NC_000004.11:g.56283332G>A , CM000666.1:g.56283332G>A	GRCh37
NC_000004.10:g.55978089G>A	NCBI36
NG_032881.1:g.26253G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.527G>A MANE Select	NP_060945.2:p.Arg176Gln
ENST00000381334.10:c.527G>A MANE Select	ENSP00000370736.5:p.Arg176Gln
NM_018475.4:c.527G>A	NP_060945.2:p.Arg176Gln
NR_073070.1:n.907G>A
NR_073070.2:n.863G>A
ENST00000381334.9:c.527G>A	ENSP00000370736.5:p.Arg176Gln
ENST00000506198.5:c.208-7373G>A	ENSP00000425449.1:n.208-7373G>A
ENST00000508404.5:c.*399G>A	ENSP00000422639.1:n.*399G>A
ENST00000508561.5:n.243G>A
ENST00000511710.1:n.651G>A
ENST00000514904.5:n.981G>A
ENST00000608091.1:c.37G>A
XM_011534394.1:c.527G>A	XP_011532696.1:p.Arg176Gln
XM_011534394.3:c.527G>A	XP_011532696.1:p.Arg176Gln
XM_017008412.1:c.338G>A	XP_016863901.1:p.Arg113Gln
XR_001741287.2:n.1064G>A