Canonical Allele Identifier: CA45684887

Gene: TMEM178A

Linked Data

• dbSNP Id: rs61358237
• MyVariant Identifiers: chr2:g.39939217_39939218insTGTA (hg19) ; chr2:g.39712077_39712078insTGTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712078_39712079insGTAT , CM000664.2:g.39712078_39712079insGTAT	GRCh38
NC_000002.11:g.39939218_39939219insGTAT , CM000664.1:g.39939218_39939219insGTAT	GRCh37
NC_000002.10:g.39792722_39792723insGTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4892_652+4893insGTAT MANE Select	ENSP00000281961.2:n.652+4892_652+4893insGTAT
ENST00000281961.2:c.652+4892_652+4893insGTAT	ENSP00000281961.2:n.652+4892_652+4893insGTAT
ENST00000413011.5:n.371+4892_371+4893insGTAT
ENST00000482239.5:n.395+4892_395+4893insGTAT
ENST00000495402.1:n.431+4892_431+4893insGTAT
ENST00000618232.1:c.*42-4932_*42-4931insGTAT	ENSP00000477622.1:n.*42-4932_*42-4931insGTAT
NM_001167959.1:c.106+4892_106+4893insGTAT	NP_001161431.1:n.106+4892_106+4893insGTAT
NM_152390.2:c.652+4892_652+4893insGTAT	NP_689603.2:n.652+4892_652+4893insGTAT
XM_005264144.1:c.515-4932_515-4931insGTAT	XP_005264201.1:n.515-4932_515-4931insGTAT
XM_005264145.1:c.401-4932_401-4931insGTAT	XP_005264202.1:n.401-4932_401-4931insGTAT
XM_017003369.1:c.*536_*537insGTAT	XP_016858858.1:n.*536_*537insGTAT
XM_017003370.2:c.106+4892_106+4893insGTAT	XP_016858859.1:n.106+4892_106+4893insGTAT
XM_017003371.1:c.106+4892_106+4893insGTAT	XP_016858860.1:n.106+4892_106+4893insGTAT
XM_024452702.1:c.401-23151_401-23150insGTAT	XP_024308470.1:n.401-23151_401-23150insGTAT
XM_024452703.1:c.106+4892_106+4893insGTAT	XP_024308471.1:n.106+4892_106+4893insGTAT
XM_024452704.1:c.106+4892_106+4893insGTAT	XP_024308472.1:n.106+4892_106+4893insGTAT
XM_024452705.1:c.106+4892_106+4893insGTAT	XP_024308473.1:n.106+4892_106+4893insGTAT
NM_152390.3:c.652+4892_652+4893insGTAT MANE Select	NP_689603.2:n.652+4892_652+4893insGTAT
NM_001167959.2:c.106+4892_106+4893insGTAT	NP_001161431.1:n.106+4892_106+4893insGTAT