Canonical Allele Identifier: CA97484491

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396286G>A , CM000666.2:g.55396286G>A	GRCh38
NC_000004.11:g.56262453G>A , CM000666.1:g.56262453G>A	GRCh37
NC_000004.10:g.55957210G>A	NCBI36
NG_032881.1:g.5374G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.97G>A MANE Select	NP_060945.2:p.Ala33Thr
ENST00000381334.10:c.97G>A MANE Select	ENSP00000370736.5:p.Ala33Thr
NM_018475.4:c.97G>A	NP_060945.2:p.Ala33Thr
NR_073070.1:n.374G>A
NR_073070.2:n.330G>A
ENST00000381334.9:c.97G>A	ENSP00000370736.5:p.Ala33Thr
ENST00000506198.5:c.97G>A	ENSP00000425449.1:p.Ala33Thr
ENST00000508404.5:c.97G>A	ENSP00000422639.1:p.Ala33Thr
ENST00000514070.1:n.36G>A
XM_011534394.1:c.97G>A	XP_011532696.1:p.Ala33Thr
XM_011534394.3:c.97G>A	XP_011532696.1:p.Ala33Thr
XM_017008412.1:c.-349G>A	XP_016863901.1:n.-349G>A
XR_001741287.2:n.634G>A