Canonical Allele Identifier: CA1246491327

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712044_39712047delinsTGTG , CM000664.2:g.39712044_39712047delinsTGTG	GRCh38
NC_000002.11:g.39939184_39939187delinsTGTG , CM000664.1:g.39939184_39939187delinsTGTG	GRCh37
NC_000002.10:g.39792688_39792691delinsTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4858_652+4861delinsTGTG MANE Select	ENSP00000281961.2:n.652+4858_652+4861delinsTGTG
ENST00000281961.2:c.652+4858_652+4861delinsTGTG	ENSP00000281961.2:n.652+4858_652+4861delinsTGTG
ENST00000413011.5:n.371+4858_371+4861delinsTGTG
ENST00000482239.5:n.395+4858_395+4861delinsTGTG
ENST00000495402.1:n.431+4858_431+4861delinsTGTG
ENST00000618232.1:c.*42-4966_*42-4963delinsTGTG	ENSP00000477622.1:n.*42-4966_*42-4963delinsTGTG
NM_001167959.1:c.106+4858_106+4861delinsTGTG	NP_001161431.1:n.106+4858_106+4861delinsTGTG
NM_152390.2:c.652+4858_652+4861delinsTGTG	NP_689603.2:n.652+4858_652+4861delinsTGTG
XM_005264144.1:c.515-4966_515-4963delinsTGTG	XP_005264201.1:n.515-4966_515-4963delinsTGTG
XM_005264145.1:c.401-4966_401-4963delinsTGTG	XP_005264202.1:n.401-4966_401-4963delinsTGTG
XM_017003369.1:c.*502_*505delinsTGTG	XP_016858858.1:n.*502_*505delinsTGTG
XM_017003370.2:c.106+4858_106+4861delinsTGTG	XP_016858859.1:n.106+4858_106+4861delinsTGTG
XM_017003371.1:c.106+4858_106+4861delinsTGTG	XP_016858860.1:n.106+4858_106+4861delinsTGTG
XM_024452702.1:c.401-23185_401-23182delinsTGTG	XP_024308470.1:n.401-23185_401-23182delinsTGTG
XM_024452703.1:c.106+4858_106+4861delinsTGTG	XP_024308471.1:n.106+4858_106+4861delinsTGTG
XM_024452704.1:c.106+4858_106+4861delinsTGTG	XP_024308472.1:n.106+4858_106+4861delinsTGTG
XM_024452705.1:c.106+4858_106+4861delinsTGTG	XP_024308473.1:n.106+4858_106+4861delinsTGTG
NM_152390.3:c.652+4858_652+4861delinsTGTG MANE Select	NP_689603.2:n.652+4858_652+4861delinsTGTG
NM_001167959.2:c.106+4858_106+4861delinsTGTG	NP_001161431.1:n.106+4858_106+4861delinsTGTG