Canonical Allele Identifier: CA768613343

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1281400973
• MyVariant Identifiers: chr2:g.39939371_39939372insA (hg19) ; chr2:g.39712231_39712232insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712238dup , CM000664.2:g.39712238dup	GRCh38
NC_000002.11:g.39939378dup , CM000664.1:g.39939378dup	GRCh37
NC_000002.10:g.39792882dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.653-4772dup MANE Select	ENSP00000281961.2:n.653-4772dup
ENST00000281961.2:c.653-4772dup	ENSP00000281961.2:n.653-4772dup
ENST00000413011.5:n.372-4772dup
ENST00000482239.5:n.396-4772dup
ENST00000495402.1:n.432-4772dup
ENST00000618232.1:c.*42-4772dup	ENSP00000477622.1:n.*42-4772dup
NM_001167959.1:c.107-4772dup	NP_001161431.1:n.107-4772dup
NM_152390.2:c.653-4772dup	NP_689603.2:n.653-4772dup
XM_005264144.1:c.515-4772dup	XP_005264201.1:n.515-4772dup
XM_005264145.1:c.401-4772dup	XP_005264202.1:n.401-4772dup
XM_017003369.1:c.*696dup	XP_016858858.1:n.*696dup
XM_017003370.2:c.107-4772dup	XP_016858859.1:n.107-4772dup
XM_017003371.1:c.107-4772dup	XP_016858860.1:n.107-4772dup
XM_024452702.1:c.401-22991dup	XP_024308470.1:n.401-22991dup
XM_024452703.1:c.107-4772dup	XP_024308471.1:n.107-4772dup
XM_024452704.1:c.107-4772dup	XP_024308472.1:n.107-4772dup
XM_024452705.1:c.107-4772dup	XP_024308473.1:n.107-4772dup
NM_152390.3:c.653-4772dup MANE Select	NP_689603.2:n.653-4772dup
NM_001167959.2:c.107-4772dup	NP_001161431.1:n.107-4772dup