Canonical Allele Identifier: CA1246491324

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712042_39712043delinsTG , CM000664.2:g.39712042_39712043delinsTG	GRCh38
NC_000002.11:g.39939182_39939183delinsTG , CM000664.1:g.39939182_39939183delinsTG	GRCh37
NC_000002.10:g.39792686_39792687delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4856_652+4857delinsTG MANE Select	ENSP00000281961.2:n.652+4856_652+4857delinsTG
ENST00000281961.2:c.652+4856_652+4857delinsTG	ENSP00000281961.2:n.652+4856_652+4857delinsTG
ENST00000413011.5:n.371+4856_371+4857delinsTG
ENST00000482239.5:n.395+4856_395+4857delinsTG
ENST00000495402.1:n.431+4856_431+4857delinsTG
ENST00000618232.1:c.*42-4968_*42-4967delinsTG	ENSP00000477622.1:n.*42-4968_*42-4967delinsTG
NM_001167959.1:c.106+4856_106+4857delinsTG	NP_001161431.1:n.106+4856_106+4857delinsTG
NM_152390.2:c.652+4856_652+4857delinsTG	NP_689603.2:n.652+4856_652+4857delinsTG
XM_005264144.1:c.515-4968_515-4967delinsTG	XP_005264201.1:n.515-4968_515-4967delinsTG
XM_005264145.1:c.401-4968_401-4967delinsTG	XP_005264202.1:n.401-4968_401-4967delinsTG
XM_017003369.1:c.*500_*501delinsTG	XP_016858858.1:n.*500_*501delinsTG
XM_017003370.2:c.106+4856_106+4857delinsTG	XP_016858859.1:n.106+4856_106+4857delinsTG
XM_017003371.1:c.106+4856_106+4857delinsTG	XP_016858860.1:n.106+4856_106+4857delinsTG
XM_024452702.1:c.401-23187_401-23186delinsTG	XP_024308470.1:n.401-23187_401-23186delinsTG
XM_024452703.1:c.106+4856_106+4857delinsTG	XP_024308471.1:n.106+4856_106+4857delinsTG
XM_024452704.1:c.106+4856_106+4857delinsTG	XP_024308472.1:n.106+4856_106+4857delinsTG
XM_024452705.1:c.106+4856_106+4857delinsTG	XP_024308473.1:n.106+4856_106+4857delinsTG
NM_152390.3:c.652+4856_652+4857delinsTG MANE Select	NP_689603.2:n.652+4856_652+4857delinsTG
NM_001167959.2:c.106+4856_106+4857delinsTG	NP_001161431.1:n.106+4856_106+4857delinsTG