Canonical Allele Identifier: CA2749592282

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712049_39712059dup , CM000664.2:g.39712049_39712059dup	GRCh38
NC_000002.11:g.39939189_39939199dup , CM000664.1:g.39939189_39939199dup	GRCh37
NC_000002.10:g.39792693_39792703dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4863_652+4873dup MANE Select	ENSP00000281961.2:n.652+4863_652+4873dup
ENST00000281961.2:c.652+4863_652+4873dup	ENSP00000281961.2:n.652+4863_652+4873dup
ENST00000413011.5:n.371+4863_371+4873dup
ENST00000482239.5:n.395+4863_395+4873dup
ENST00000495402.1:n.431+4863_431+4873dup
ENST00000618232.1:c.*42-4961_*42-4951dup	ENSP00000477622.1:n.*42-4961_*42-4951dup
NM_001167959.1:c.106+4863_106+4873dup	NP_001161431.1:n.106+4863_106+4873dup
NM_152390.2:c.652+4863_652+4873dup	NP_689603.2:n.652+4863_652+4873dup
XM_005264144.1:c.515-4961_515-4951dup	XP_005264201.1:n.515-4961_515-4951dup
XM_005264145.1:c.401-4961_401-4951dup	XP_005264202.1:n.401-4961_401-4951dup
XM_017003369.1:c.*507_*517dup	XP_016858858.1:n.*507_*517dup
XM_017003370.2:c.106+4863_106+4873dup	XP_016858859.1:n.106+4863_106+4873dup
XM_017003371.1:c.106+4863_106+4873dup	XP_016858860.1:n.106+4863_106+4873dup
XM_024452702.1:c.401-23180_401-23170dup	XP_024308470.1:n.401-23180_401-23170dup
XM_024452703.1:c.106+4863_106+4873dup	XP_024308471.1:n.106+4863_106+4873dup
XM_024452704.1:c.106+4863_106+4873dup	XP_024308472.1:n.106+4863_106+4873dup
XM_024452705.1:c.106+4863_106+4873dup	XP_024308473.1:n.106+4863_106+4873dup
NM_152390.3:c.652+4863_652+4873dup MANE Select	NP_689603.2:n.652+4863_652+4873dup
NM_001167959.2:c.106+4863_106+4873dup	NP_001161431.1:n.106+4863_106+4873dup