Canonical Allele Identifier: CA1459091627

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55423960A= , CM000666.2:g.55423960A=	GRCh38
NC_000004.11:g.56290127A= , CM000666.1:g.56290127A=	GRCh37
NC_000004.10:g.55984884A=	NCBI36
NG_032881.1:g.33048A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381334.10:c.793-578A= MANE Select	ENSP00000370736.5:n.793-578A=
ENST00000381334.9:c.793-578A=	ENSP00000370736.5:n.793-578A=
ENST00000506103.2:c.247-578A=
ENST00000506198.5:c.208-578A=	ENSP00000425449.1:n.208-578A=
ENST00000508404.5:c.*665-578A=	ENSP00000422639.1:n.*665-578A=
ENST00000508561.5:n.489-578A=
ENST00000509575.1:n.296-578A=
ENST00000514904.5:n.1247-578A=
ENST00000515591.1:n.847A=
ENST00000608091.1:c.303-578A=
NM_018475.4:c.793-578A=	NP_060945.2:n.793-578A=
NR_073070.1:n.1173-578A=
XM_011534394.1:c.793-578A=	XP_011532696.1:n.793-578A=
XM_011534394.3:c.793-578A=	XP_011532696.1:n.793-578A=
XM_017008412.1:c.604-578A=	XP_016863901.1:n.604-578A=
XR_001741287.2:n.1509-578A=
NM_018475.5:c.793-578A= MANE Select	NP_060945.2:n.793-578A=
NR_073070.2:n.1129-578A=