Canonical Allele Identifier: CA2553307235

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39711928_39711936dup , CM000664.2:g.39711928_39711936dup	GRCh38
NC_000002.11:g.39939068_39939076dup , CM000664.1:g.39939068_39939076dup	GRCh37
NC_000002.10:g.39792572_39792580dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4742_652+4750dup MANE Select	ENSP00000281961.2:n.652+4742_652+4750dup
ENST00000281961.2:c.652+4742_652+4750dup	ENSP00000281961.2:n.652+4742_652+4750dup
ENST00000413011.5:n.371+4742_371+4750dup
ENST00000482239.5:n.395+4742_395+4750dup
ENST00000495402.1:n.431+4742_431+4750dup
ENST00000618232.1:c.*42-5082_*42-5074dup	ENSP00000477622.1:n.*42-5082_*42-5074dup
NM_001167959.1:c.106+4742_106+4750dup	NP_001161431.1:n.106+4742_106+4750dup
NM_152390.2:c.652+4742_652+4750dup	NP_689603.2:n.652+4742_652+4750dup
XM_005264144.1:c.515-5082_515-5074dup	XP_005264201.1:n.515-5082_515-5074dup
XM_005264145.1:c.401-5082_401-5074dup	XP_005264202.1:n.401-5082_401-5074dup
XM_017003369.1:c.*386_*394dup	XP_016858858.1:n.*386_*394dup
XM_017003370.2:c.106+4742_106+4750dup	XP_016858859.1:n.106+4742_106+4750dup
XM_017003371.1:c.106+4742_106+4750dup	XP_016858860.1:n.106+4742_106+4750dup
XM_024452702.1:c.401-23301_401-23293dup	XP_024308470.1:n.401-23301_401-23293dup
XM_024452703.1:c.106+4742_106+4750dup	XP_024308471.1:n.106+4742_106+4750dup
XM_024452704.1:c.106+4742_106+4750dup	XP_024308472.1:n.106+4742_106+4750dup
XM_024452705.1:c.106+4742_106+4750dup	XP_024308473.1:n.106+4742_106+4750dup
NM_152390.3:c.652+4742_652+4750dup MANE Select	NP_689603.2:n.652+4742_652+4750dup
NM_001167959.2:c.106+4742_106+4750dup	NP_001161431.1:n.106+4742_106+4750dup