Canonical Allele Identifier: CA1246491280

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39711972_39711973delinsTG , CM000664.2:g.39711972_39711973delinsTG	GRCh38
NC_000002.11:g.39939112_39939113delinsTG , CM000664.1:g.39939112_39939113delinsTG	GRCh37
NC_000002.10:g.39792616_39792617delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4786_652+4787delinsTG MANE Select	ENSP00000281961.2:n.652+4786_652+4787delinsTG
ENST00000281961.2:c.652+4786_652+4787delinsTG	ENSP00000281961.2:n.652+4786_652+4787delinsTG
ENST00000413011.5:n.371+4786_371+4787delinsTG
ENST00000482239.5:n.395+4786_395+4787delinsTG
ENST00000495402.1:n.431+4786_431+4787delinsTG
ENST00000618232.1:c.*42-5038_*42-5037delinsTG	ENSP00000477622.1:n.*42-5038_*42-5037delinsTG
NM_001167959.1:c.106+4786_106+4787delinsTG	NP_001161431.1:n.106+4786_106+4787delinsTG
NM_152390.2:c.652+4786_652+4787delinsTG	NP_689603.2:n.652+4786_652+4787delinsTG
XM_005264144.1:c.515-5038_515-5037delinsTG	XP_005264201.1:n.515-5038_515-5037delinsTG
XM_005264145.1:c.401-5038_401-5037delinsTG	XP_005264202.1:n.401-5038_401-5037delinsTG
XM_017003369.1:c.*430_*431delinsTG	XP_016858858.1:n.*430_*431delinsTG
XM_017003370.2:c.106+4786_106+4787delinsTG	XP_016858859.1:n.106+4786_106+4787delinsTG
XM_017003371.1:c.106+4786_106+4787delinsTG	XP_016858860.1:n.106+4786_106+4787delinsTG
XM_024452702.1:c.401-23257_401-23256delinsTG	XP_024308470.1:n.401-23257_401-23256delinsTG
XM_024452703.1:c.106+4786_106+4787delinsTG	XP_024308471.1:n.106+4786_106+4787delinsTG
XM_024452704.1:c.106+4786_106+4787delinsTG	XP_024308472.1:n.106+4786_106+4787delinsTG
XM_024452705.1:c.106+4786_106+4787delinsTG	XP_024308473.1:n.106+4786_106+4787delinsTG
NM_152390.3:c.652+4786_652+4787delinsTG MANE Select	NP_689603.2:n.652+4786_652+4787delinsTG
NM_001167959.2:c.106+4786_106+4787delinsTG	NP_001161431.1:n.106+4786_106+4787delinsTG