Canonical Allele Identifier: CA1029629155

Gene: TMEM178A

Linked Data

• dbSNP Id: rs70957121
• gnomAD v3: 2-39712078-T-TGTGTGTGTGTGTGTGTG
• gnomAD v4: 2-39712078-T-TGTGTGTGTGTGTGTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712078_39712079insGTGTGTGTGTGTGTGTG , CM000664.2:g.39712078_39712079insGTGTGTGTGTGTGTGTG	GRCh38
NC_000002.11:g.39939218_39939219insGTGTGTGTGTGTGTGTG , CM000664.1:g.39939218_39939219insGTGTGTGTGTGTGTGTG	GRCh37
NC_000002.10:g.39792722_39792723insGTGTGTGTGTGTGTGTG	NCBI36

Transcript Alleles

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