Canonical Allele Identifier: CA1246491334

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1672332003

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712052_39712053insCTGT , CM000664.2:g.39712052_39712053insCTGT	GRCh38
NC_000002.11:g.39939192_39939193insCTGT , CM000664.1:g.39939192_39939193insCTGT	GRCh37
NC_000002.10:g.39792696_39792697insCTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4866_652+4867insCTGT MANE Select	ENSP00000281961.2:n.652+4866_652+4867insCTGT
ENST00000281961.2:c.652+4866_652+4867insCTGT	ENSP00000281961.2:n.652+4866_652+4867insCTGT
ENST00000413011.5:n.371+4866_371+4867insCTGT
ENST00000482239.5:n.395+4866_395+4867insCTGT
ENST00000495402.1:n.431+4866_431+4867insCTGT
ENST00000618232.1:c.*42-4958_*42-4957insCTGT	ENSP00000477622.1:n.*42-4958_*42-4957insCTGT
NM_001167959.1:c.106+4866_106+4867insCTGT	NP_001161431.1:n.106+4866_106+4867insCTGT
NM_152390.2:c.652+4866_652+4867insCTGT	NP_689603.2:n.652+4866_652+4867insCTGT
XM_005264144.1:c.515-4958_515-4957insCTGT	XP_005264201.1:n.515-4958_515-4957insCTGT
XM_005264145.1:c.401-4958_401-4957insCTGT	XP_005264202.1:n.401-4958_401-4957insCTGT
XM_017003369.1:c.*510_*511insCTGT	XP_016858858.1:n.*510_*511insCTGT
XM_017003370.2:c.106+4866_106+4867insCTGT	XP_016858859.1:n.106+4866_106+4867insCTGT
XM_017003371.1:c.106+4866_106+4867insCTGT	XP_016858860.1:n.106+4866_106+4867insCTGT
XM_024452702.1:c.401-23177_401-23176insCTGT	XP_024308470.1:n.401-23177_401-23176insCTGT
XM_024452703.1:c.106+4866_106+4867insCTGT	XP_024308471.1:n.106+4866_106+4867insCTGT
XM_024452704.1:c.106+4866_106+4867insCTGT	XP_024308472.1:n.106+4866_106+4867insCTGT
XM_024452705.1:c.106+4866_106+4867insCTGT	XP_024308473.1:n.106+4866_106+4867insCTGT
NM_152390.3:c.652+4866_652+4867insCTGT MANE Select	NP_689603.2:n.652+4866_652+4867insCTGT
NM_001167959.2:c.106+4866_106+4867insCTGT	NP_001161431.1:n.106+4866_106+4867insCTGT