Canonical Allele Identifier: CA1029629000

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1672327342
• gnomAD v3: 2-39712040-T-TG
• gnomAD v4: 2-39712040-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712040_39712041insG , CM000664.2:g.39712040_39712041insG	GRCh38
NC_000002.11:g.39939180_39939181insG , CM000664.1:g.39939180_39939181insG	GRCh37
NC_000002.10:g.39792684_39792685insG	NCBI36

Transcript Alleles

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