Canonical Allele Identifier: CA1029629191
Gene: TMEM178A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39712081_39712082insTGTGTGTG , CM000664.2:g.39712081_39712082insTGTGTGTG GRCh38
NC_000002.11:g.39939221_39939222insTGTGTGTG , CM000664.1:g.39939221_39939222insTGTGTGTG GRCh37
NC_000002.10:g.39792725_39792726insTGTGTGTG NCBI36

Transcript Alleles

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