Canonical Allele Identifier: CA1029629192

Gene: TMEM178A

Linked Data

• gnomAD v3: 2-39712080-A-AGTGT
• gnomAD v4: 2-39712080-A-AGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712081_39712082insTGTG , CM000664.2:g.39712081_39712082insTGTG	GRCh38
NC_000002.11:g.39939221_39939222insTGTG , CM000664.1:g.39939221_39939222insTGTG	GRCh37
NC_000002.10:g.39792725_39792726insTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4895_652+4896insTGTG MANE Select	ENSP00000281961.2:n.652+4895_652+4896insTGTG
ENST00000281961.2:c.652+4895_652+4896insTGTG	ENSP00000281961.2:n.652+4895_652+4896insTGTG
ENST00000413011.5:n.371+4895_371+4896insTGTG
ENST00000482239.5:n.395+4895_395+4896insTGTG
ENST00000495402.1:n.431+4895_431+4896insTGTG
ENST00000618232.1:c.*42-4929_*42-4928insTGTG	ENSP00000477622.1:n.*42-4929_*42-4928insTGTG
NM_001167959.1:c.106+4895_106+4896insTGTG	NP_001161431.1:n.106+4895_106+4896insTGTG
NM_152390.2:c.652+4895_652+4896insTGTG	NP_689603.2:n.652+4895_652+4896insTGTG
XM_005264144.1:c.515-4929_515-4928insTGTG	XP_005264201.1:n.515-4929_515-4928insTGTG
XM_005264145.1:c.401-4929_401-4928insTGTG	XP_005264202.1:n.401-4929_401-4928insTGTG
XM_017003369.1:c.*539_*540insTGTG	XP_016858858.1:n.*539_*540insTGTG
XM_017003370.2:c.106+4895_106+4896insTGTG	XP_016858859.1:n.106+4895_106+4896insTGTG
XM_017003371.1:c.106+4895_106+4896insTGTG	XP_016858860.1:n.106+4895_106+4896insTGTG
XM_024452702.1:c.401-23148_401-23147insTGTG	XP_024308470.1:n.401-23148_401-23147insTGTG
XM_024452703.1:c.106+4895_106+4896insTGTG	XP_024308471.1:n.106+4895_106+4896insTGTG
XM_024452704.1:c.106+4895_106+4896insTGTG	XP_024308472.1:n.106+4895_106+4896insTGTG
XM_024452705.1:c.106+4895_106+4896insTGTG	XP_024308473.1:n.106+4895_106+4896insTGTG
NM_152390.3:c.652+4895_652+4896insTGTG MANE Select	NP_689603.2:n.652+4895_652+4896insTGTG
NM_001167959.2:c.106+4895_106+4896insTGTG	NP_001161431.1:n.106+4895_106+4896insTGTG