Canonical Allele Identifier: CA439480344

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55417133A>G , CM000666.2:g.55417133A>G	GRCh38
NC_000004.11:g.56283300A>G , CM000666.1:g.56283300A>G	GRCh37
NC_000004.10:g.55978057A>G	NCBI36
NG_032881.1:g.26221A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.495A>G MANE Select	NP_060945.2:p.Val165=
ENST00000381334.10:c.495A>G MANE Select	ENSP00000370736.5:p.Val165=
NM_018475.4:c.495A>G	NP_060945.2:p.Val165=
NR_073070.1:n.875A>G
NR_073070.2:n.831A>G
ENST00000381334.9:c.495A>G	ENSP00000370736.5:p.Val165=
ENST00000506198.5:c.208-7405A>G	ENSP00000425449.1:n.208-7405A>G
ENST00000508404.5:c.*367A>G	ENSP00000422639.1:n.*367A>G
ENST00000508561.5:n.211A>G
ENST00000511710.1:n.619A>G
ENST00000514904.5:n.949A>G
ENST00000608091.1:c.5A>G
XM_011534394.1:c.495A>G	XP_011532696.1:p.Val165=
XM_011534394.3:c.495A>G	XP_011532696.1:p.Val165=
XM_017008412.1:c.306A>G	XP_016863901.1:p.Val102=
XR_001741287.2:n.1032A>G