Canonical Allele Identifier: CA2699115307

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1412951521

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712079_39712080insG , CM000664.2:g.39712079_39712080insG	GRCh38
NC_000002.11:g.39939219_39939220insG , CM000664.1:g.39939219_39939220insG	GRCh37
NC_000002.10:g.39792723_39792724insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4893_652+4894insG MANE Select	ENSP00000281961.2:n.652+4893_652+4894insG
ENST00000281961.2:c.652+4893_652+4894insG	ENSP00000281961.2:n.652+4893_652+4894insG
ENST00000413011.5:n.371+4893_371+4894insG
ENST00000482239.5:n.395+4893_395+4894insG
ENST00000495402.1:n.431+4893_431+4894insG
ENST00000618232.1:c.*42-4931_*42-4930insG	ENSP00000477622.1:n.*42-4931_*42-4930insG
NM_001167959.1:c.106+4893_106+4894insG	NP_001161431.1:n.106+4893_106+4894insG
NM_152390.2:c.652+4893_652+4894insG	NP_689603.2:n.652+4893_652+4894insG
XM_005264144.1:c.515-4931_515-4930insG	XP_005264201.1:n.515-4931_515-4930insG
XM_005264145.1:c.401-4931_401-4930insG	XP_005264202.1:n.401-4931_401-4930insG
XM_017003369.1:c.*537_*538insG	XP_016858858.1:n.*537_*538insG
XM_017003370.2:c.106+4893_106+4894insG	XP_016858859.1:n.106+4893_106+4894insG
XM_017003371.1:c.106+4893_106+4894insG	XP_016858860.1:n.106+4893_106+4894insG
XM_024452702.1:c.401-23150_401-23149insG	XP_024308470.1:n.401-23150_401-23149insG
XM_024452703.1:c.106+4893_106+4894insG	XP_024308471.1:n.106+4893_106+4894insG
XM_024452704.1:c.106+4893_106+4894insG	XP_024308472.1:n.106+4893_106+4894insG
XM_024452705.1:c.106+4893_106+4894insG	XP_024308473.1:n.106+4893_106+4894insG
NM_152390.3:c.652+4893_652+4894insG MANE Select	NP_689603.2:n.652+4893_652+4894insG
NM_001167959.2:c.106+4893_106+4894insG	NP_001161431.1:n.106+4893_106+4894insG