Canonical Allele Identifier: CA356958876

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396332C>T , CM000666.2:g.55396332C>T	GRCh38
NC_000004.11:g.56262499C>T , CM000666.1:g.56262499C>T	GRCh37
NC_000004.10:g.55957256C>T	NCBI36
NG_032881.1:g.5420C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.143C>T MANE Select	NP_060945.2:p.Ala48Val
ENST00000381334.10:c.143C>T MANE Select	ENSP00000370736.5:p.Ala48Val
NM_018475.4:c.143C>T	NP_060945.2:p.Ala48Val
NR_073070.1:n.420C>T
NR_073070.2:n.376C>T
ENST00000381334.9:c.143C>T	ENSP00000370736.5:p.Ala48Val
ENST00000506198.5:c.143C>T	ENSP00000425449.1:p.Ala48Val
ENST00000508404.5:c.143C>T	ENSP00000422639.1:p.Ala48Val
ENST00000514070.1:n.82C>T
XM_011534394.1:c.143C>T	XP_011532696.1:p.Ala48Val
XM_011534394.3:c.143C>T	XP_011532696.1:p.Ala48Val
XM_017008412.1:c.-303C>T	XP_016863901.1:n.-303C>T
XR_001741287.2:n.680C>T