Canonical Allele Identifier: CA356958987

Gene: TMEM165

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55396385G>T , CM000666.2:g.55396385G>T	GRCh38
NC_000004.11:g.56262552G>T , CM000666.1:g.56262552G>T	GRCh37
NC_000004.10:g.55957309G>T	NCBI36
NG_032881.1:g.5473G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018475.5:c.196G>T MANE Select	NP_060945.2:p.Ala66Ser
ENST00000381334.10:c.196G>T MANE Select	ENSP00000370736.5:p.Ala66Ser
NM_018475.4:c.196G>T	NP_060945.2:p.Ala66Ser
NR_073070.1:n.473G>T
NR_073070.2:n.429G>T
ENST00000381334.9:c.196G>T	ENSP00000370736.5:p.Ala66Ser
ENST00000506198.5:c.196G>T	ENSP00000425449.1:p.Ala66Ser
ENST00000508404.5:c.196G>T	ENSP00000422639.1:p.Ala66Ser
ENST00000514070.1:n.135G>T
XM_011534394.1:c.196G>T	XP_011532696.1:p.Ala66Ser
XM_011534394.3:c.196G>T	XP_011532696.1:p.Ala66Ser
XM_017008412.1:c.-250G>T	XP_016863901.1:n.-250G>T
XR_001741287.2:n.733G>T