Canonical Allele Identifier: CA1246491302

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712011_39712012delinsTG , CM000664.2:g.39712011_39712012delinsTG	GRCh38
NC_000002.11:g.39939151_39939152delinsTG , CM000664.1:g.39939151_39939152delinsTG	GRCh37
NC_000002.10:g.39792655_39792656delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4825_652+4826delinsTG MANE Select	ENSP00000281961.2:n.652+4825_652+4826delinsTG
ENST00000281961.2:c.652+4825_652+4826delinsTG	ENSP00000281961.2:n.652+4825_652+4826delinsTG
ENST00000413011.5:n.371+4825_371+4826delinsTG
ENST00000482239.5:n.395+4825_395+4826delinsTG
ENST00000495402.1:n.431+4825_431+4826delinsTG
ENST00000618232.1:c.*42-4999_*42-4998delinsTG	ENSP00000477622.1:n.*42-4999_*42-4998delinsTG
NM_001167959.1:c.106+4825_106+4826delinsTG	NP_001161431.1:n.106+4825_106+4826delinsTG
NM_152390.2:c.652+4825_652+4826delinsTG	NP_689603.2:n.652+4825_652+4826delinsTG
XM_005264144.1:c.515-4999_515-4998delinsTG	XP_005264201.1:n.515-4999_515-4998delinsTG
XM_005264145.1:c.401-4999_401-4998delinsTG	XP_005264202.1:n.401-4999_401-4998delinsTG
XM_017003369.1:c.*469_*470delinsTG	XP_016858858.1:n.*469_*470delinsTG
XM_017003370.2:c.106+4825_106+4826delinsTG	XP_016858859.1:n.106+4825_106+4826delinsTG
XM_017003371.1:c.106+4825_106+4826delinsTG	XP_016858860.1:n.106+4825_106+4826delinsTG
XM_024452702.1:c.401-23218_401-23217delinsTG	XP_024308470.1:n.401-23218_401-23217delinsTG
XM_024452703.1:c.106+4825_106+4826delinsTG	XP_024308471.1:n.106+4825_106+4826delinsTG
XM_024452704.1:c.106+4825_106+4826delinsTG	XP_024308472.1:n.106+4825_106+4826delinsTG
XM_024452705.1:c.106+4825_106+4826delinsTG	XP_024308473.1:n.106+4825_106+4826delinsTG
NM_152390.3:c.652+4825_652+4826delinsTG MANE Select	NP_689603.2:n.652+4825_652+4826delinsTG
NM_001167959.2:c.106+4825_106+4826delinsTG	NP_001161431.1:n.106+4825_106+4826delinsTG