Canonical Allele Identifier: CA768613236

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1449061075
• MyVariant Identifiers: chr2:g.39939195_39939196insTGTA (hg19) ; chr2:g.39712055_39712056insTGTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712058_39712059insATGT , CM000664.2:g.39712058_39712059insATGT	GRCh38
NC_000002.11:g.39939198_39939199insATGT , CM000664.1:g.39939198_39939199insATGT	GRCh37
NC_000002.10:g.39792702_39792703insATGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4872_652+4873insATGT MANE Select	ENSP00000281961.2:n.652+4872_652+4873insATGT
ENST00000281961.2:c.652+4872_652+4873insATGT	ENSP00000281961.2:n.652+4872_652+4873insATGT
ENST00000413011.5:n.371+4872_371+4873insATGT
ENST00000482239.5:n.395+4872_395+4873insATGT
ENST00000495402.1:n.431+4872_431+4873insATGT
ENST00000618232.1:c.*42-4952_*42-4951insATGT	ENSP00000477622.1:n.*42-4952_*42-4951insATGT
NM_001167959.1:c.106+4872_106+4873insATGT	NP_001161431.1:n.106+4872_106+4873insATGT
NM_152390.2:c.652+4872_652+4873insATGT	NP_689603.2:n.652+4872_652+4873insATGT
XM_005264144.1:c.515-4952_515-4951insATGT	XP_005264201.1:n.515-4952_515-4951insATGT
XM_005264145.1:c.401-4952_401-4951insATGT	XP_005264202.1:n.401-4952_401-4951insATGT
XM_017003369.1:c.*516_*517insATGT	XP_016858858.1:n.*516_*517insATGT
XM_017003370.2:c.106+4872_106+4873insATGT	XP_016858859.1:n.106+4872_106+4873insATGT
XM_017003371.1:c.106+4872_106+4873insATGT	XP_016858860.1:n.106+4872_106+4873insATGT
XM_024452702.1:c.401-23171_401-23170insATGT	XP_024308470.1:n.401-23171_401-23170insATGT
XM_024452703.1:c.106+4872_106+4873insATGT	XP_024308471.1:n.106+4872_106+4873insATGT
XM_024452704.1:c.106+4872_106+4873insATGT	XP_024308472.1:n.106+4872_106+4873insATGT
XM_024452705.1:c.106+4872_106+4873insATGT	XP_024308473.1:n.106+4872_106+4873insATGT
NM_152390.3:c.652+4872_652+4873insATGT MANE Select	NP_689603.2:n.652+4872_652+4873insATGT
NM_001167959.2:c.106+4872_106+4873insATGT	NP_001161431.1:n.106+4872_106+4873insATGT