Canonical Allele Identifier: CA531977326

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1181400872
• gnomAD v2: 2-39939224-T-TG
• gnomAD v3: 2-39712084-T-TG
• gnomAD v4: 2-39712084-T-TG
• MyVariant Identifiers: chr2:g.39939224_39939225insG (hg19) ; chr2:g.39712084_39712085insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712084_39712085insG , CM000664.2:g.39712084_39712085insG	GRCh38
NC_000002.11:g.39939224_39939225insG , CM000664.1:g.39939224_39939225insG	GRCh37
NC_000002.10:g.39792728_39792729insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4898_652+4899insG MANE Select	ENSP00000281961.2:n.652+4898_652+4899insG
ENST00000281961.2:c.652+4898_652+4899insG	ENSP00000281961.2:n.652+4898_652+4899insG
ENST00000413011.5:n.371+4898_371+4899insG
ENST00000482239.5:n.395+4898_395+4899insG
ENST00000495402.1:n.431+4898_431+4899insG
ENST00000618232.1:c.*42-4926_*42-4925insG	ENSP00000477622.1:n.*42-4926_*42-4925insG
NM_001167959.1:c.106+4898_106+4899insG	NP_001161431.1:n.106+4898_106+4899insG
NM_152390.2:c.652+4898_652+4899insG	NP_689603.2:n.652+4898_652+4899insG
XM_005264144.1:c.515-4926_515-4925insG	XP_005264201.1:n.515-4926_515-4925insG
XM_005264145.1:c.401-4926_401-4925insG	XP_005264202.1:n.401-4926_401-4925insG
XM_017003369.1:c.*542_*543insG	XP_016858858.1:n.*542_*543insG
XM_017003370.2:c.106+4898_106+4899insG	XP_016858859.1:n.106+4898_106+4899insG
XM_017003371.1:c.106+4898_106+4899insG	XP_016858860.1:n.106+4898_106+4899insG
XM_024452702.1:c.401-23145_401-23144insG	XP_024308470.1:n.401-23145_401-23144insG
XM_024452703.1:c.106+4898_106+4899insG	XP_024308471.1:n.106+4898_106+4899insG
XM_024452704.1:c.106+4898_106+4899insG	XP_024308472.1:n.106+4898_106+4899insG
XM_024452705.1:c.106+4898_106+4899insG	XP_024308473.1:n.106+4898_106+4899insG
NM_152390.3:c.652+4898_652+4899insG MANE Select	NP_689603.2:n.652+4898_652+4899insG
NM_001167959.2:c.106+4898_106+4899insG	NP_001161431.1:n.106+4898_106+4899insG