Canonical Allele Identifier: CA2925601

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55424576C>T , CM000666.2:g.55424576C>T	GRCh38
NC_000004.11:g.56290743C>T , CM000666.1:g.56290743C>T	GRCh37
NC_000004.10:g.55985500C>T	NCBI36
NG_032881.1:g.33664C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.831C>T MANE Select	NP_060945.2:p.His277=
ENST00000381334.10:c.831C>T MANE Select	ENSP00000370736.5:p.His277=
NM_018475.4:c.831C>T	NP_060945.2:p.His277=
NR_073070.1:n.1211C>T
NR_073070.2:n.1167C>T
ENST00000381334.9:c.831C>T	ENSP00000370736.5:p.His277=
ENST00000506103.2:c.285C>T
ENST00000506198.5:c.246C>T	ENSP00000425449.1:p.His82=
ENST00000508404.5:c.*703C>T	ENSP00000422639.1:n.*703C>T
ENST00000508561.5:n.527C>T
ENST00000509575.1:n.334C>T
ENST00000514904.5:n.1285C>T
ENST00000515591.1:n.1463C>T
ENST00000608091.1:c.341C>T
XM_011534394.1:c.831C>T	XP_011532696.1:p.His277=
XM_011534394.3:c.831C>T	XP_011532696.1:p.His277=
XM_017008412.1:c.642C>T	XP_016863901.1:p.His214=
XR_001741287.2:n.1547C>T