Canonical Allele Identifier: CA768613080

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1284524292
• MyVariant Identifiers: chr2:g.39939179_39939180insTG (hg19) ; chr2:g.39712039_39712040insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712040_39712041insGT , CM000664.2:g.39712040_39712041insGT	GRCh38
NC_000002.11:g.39939180_39939181insGT , CM000664.1:g.39939180_39939181insGT	GRCh37
NC_000002.10:g.39792684_39792685insGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4854_652+4855insGT MANE Select	ENSP00000281961.2:n.652+4854_652+4855insGT
ENST00000281961.2:c.652+4854_652+4855insGT	ENSP00000281961.2:n.652+4854_652+4855insGT
ENST00000413011.5:n.371+4854_371+4855insGT
ENST00000482239.5:n.395+4854_395+4855insGT
ENST00000495402.1:n.431+4854_431+4855insGT
ENST00000618232.1:c.*42-4970_*42-4969insGT	ENSP00000477622.1:n.*42-4970_*42-4969insGT
NM_001167959.1:c.106+4854_106+4855insGT	NP_001161431.1:n.106+4854_106+4855insGT
NM_152390.2:c.652+4854_652+4855insGT	NP_689603.2:n.652+4854_652+4855insGT
XM_005264144.1:c.515-4970_515-4969insGT	XP_005264201.1:n.515-4970_515-4969insGT
XM_005264145.1:c.401-4970_401-4969insGT	XP_005264202.1:n.401-4970_401-4969insGT
XM_017003369.1:c.*498_*499insGT	XP_016858858.1:n.*498_*499insGT
XM_017003370.2:c.106+4854_106+4855insGT	XP_016858859.1:n.106+4854_106+4855insGT
XM_017003371.1:c.106+4854_106+4855insGT	XP_016858860.1:n.106+4854_106+4855insGT
XM_024452702.1:c.401-23189_401-23188insGT	XP_024308470.1:n.401-23189_401-23188insGT
XM_024452703.1:c.106+4854_106+4855insGT	XP_024308471.1:n.106+4854_106+4855insGT
XM_024452704.1:c.106+4854_106+4855insGT	XP_024308472.1:n.106+4854_106+4855insGT
XM_024452705.1:c.106+4854_106+4855insGT	XP_024308473.1:n.106+4854_106+4855insGT
NM_152390.3:c.652+4854_652+4855insGT MANE Select	NP_689603.2:n.652+4854_652+4855insGT
NM_001167959.2:c.106+4854_106+4855insGT	NP_001161431.1:n.106+4854_106+4855insGT