Canonical Allele Identifier: CA1246491314

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712039_39712043delinsTTTTG , CM000664.2:g.39712039_39712043delinsTTTTG	GRCh38
NC_000002.11:g.39939179_39939183delinsTTTTG , CM000664.1:g.39939179_39939183delinsTTTTG	GRCh37
NC_000002.10:g.39792683_39792687delinsTTTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4853_652+4857delinsTTTTG MANE Select	ENSP00000281961.2:n.652+4853_652+4857delinsTTTTG
ENST00000281961.2:c.652+4853_652+4857delinsTTTTG	ENSP00000281961.2:n.652+4853_652+4857delinsTTTTG
ENST00000413011.5:n.371+4853_371+4857delinsTTTTG
ENST00000482239.5:n.395+4853_395+4857delinsTTTTG
ENST00000495402.1:n.431+4853_431+4857delinsTTTTG
ENST00000618232.1:c.*42-4971_*42-4967delinsTTTTG	ENSP00000477622.1:n.*42-4971_*42-4967delinsTTTTG
NM_001167959.1:c.106+4853_106+4857delinsTTTTG	NP_001161431.1:n.106+4853_106+4857delinsTTTTG
NM_152390.2:c.652+4853_652+4857delinsTTTTG	NP_689603.2:n.652+4853_652+4857delinsTTTTG
XM_005264144.1:c.515-4971_515-4967delinsTTTTG	XP_005264201.1:n.515-4971_515-4967delinsTTTTG
XM_005264145.1:c.401-4971_401-4967delinsTTTTG	XP_005264202.1:n.401-4971_401-4967delinsTTTTG
XM_017003369.1:c.*497_*501delinsTTTTG	XP_016858858.1:n.*497_*501delinsTTTTG
XM_017003370.2:c.106+4853_106+4857delinsTTTTG	XP_016858859.1:n.106+4853_106+4857delinsTTTTG
XM_017003371.1:c.106+4853_106+4857delinsTTTTG	XP_016858860.1:n.106+4853_106+4857delinsTTTTG
XM_024452702.1:c.401-23190_401-23186delinsTTTTG	XP_024308470.1:n.401-23190_401-23186delinsTTTTG
XM_024452703.1:c.106+4853_106+4857delinsTTTTG	XP_024308471.1:n.106+4853_106+4857delinsTTTTG
XM_024452704.1:c.106+4853_106+4857delinsTTTTG	XP_024308472.1:n.106+4853_106+4857delinsTTTTG
XM_024452705.1:c.106+4853_106+4857delinsTTTTG	XP_024308473.1:n.106+4853_106+4857delinsTTTTG
NM_152390.3:c.652+4853_652+4857delinsTTTTG MANE Select	NP_689603.2:n.652+4853_652+4857delinsTTTTG
NM_001167959.2:c.106+4853_106+4857delinsTTTTG	NP_001161431.1:n.106+4853_106+4857delinsTTTTG