Canonical Allele Identifier: CA1459091637

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55423977C= , CM000666.2:g.55423977C=	GRCh38
NC_000004.11:g.56290144C= , CM000666.1:g.56290144C=	GRCh37
NC_000004.10:g.55984901C=	NCBI36
NG_032881.1:g.33065C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381334.10:c.793-561C= MANE Select	ENSP00000370736.5:n.793-561C=
ENST00000381334.9:c.793-561C=	ENSP00000370736.5:n.793-561C=
ENST00000506103.2:c.247-561C=
ENST00000506198.5:c.208-561C=	ENSP00000425449.1:n.208-561C=
ENST00000508404.5:c.*665-561C=	ENSP00000422639.1:n.*665-561C=
ENST00000508561.5:n.489-561C=
ENST00000509575.1:n.296-561C=
ENST00000514904.5:n.1247-561C=
ENST00000515591.1:n.864C=
ENST00000608091.1:c.303-561C=
NM_018475.4:c.793-561C=	NP_060945.2:n.793-561C=
NR_073070.1:n.1173-561C=
XM_011534394.1:c.793-561C=	XP_011532696.1:n.793-561C=
XM_011534394.3:c.793-561C=	XP_011532696.1:n.793-561C=
XM_017008412.1:c.604-561C=	XP_016863901.1:n.604-561C=
XR_001741287.2:n.1509-561C=
NM_018475.5:c.793-561C= MANE Select	NP_060945.2:n.793-561C=
NR_073070.2:n.1129-561C=