Canonical Allele Identifier: CA1246491338

Gene: TMEM178A

Linked Data

• dbSNP Id: rs1672332427

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712063_39712064insCGTGTGTGTGTG , CM000664.2:g.39712063_39712064insCGTGTGTGTGTG	GRCh38
NC_000002.11:g.39939203_39939204insCGTGTGTGTGTG , CM000664.1:g.39939203_39939204insCGTGTGTGTGTG	GRCh37
NC_000002.10:g.39792707_39792708insCGTGTGTGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.652+4877_652+4878insCGTGTGTGTGTG MANE Select	ENSP00000281961.2:n.652+4877_652+4878insCGTGTGTGTGTG
ENST00000281961.2:c.652+4877_652+4878insCGTGTGTGTGTG	ENSP00000281961.2:n.652+4877_652+4878insCGTGTGTGTGTG
ENST00000413011.5:n.371+4877_371+4878insCGTGTGTGTGTG
ENST00000482239.5:n.395+4877_395+4878insCGTGTGTGTGTG
ENST00000495402.1:n.431+4877_431+4878insCGTGTGTGTGTG
ENST00000618232.1:c.*42-4947_*42-4946insCGTGTGTGTGTG	ENSP00000477622.1:n.*42-4947_*42-4946insCGTGTGTGTGTG
NM_001167959.1:c.106+4877_106+4878insCGTGTGTGTGTG	NP_001161431.1:n.106+4877_106+4878insCGTGTGTGTGTG
NM_152390.2:c.652+4877_652+4878insCGTGTGTGTGTG	NP_689603.2:n.652+4877_652+4878insCGTGTGTGTGTG
XM_005264144.1:c.515-4947_515-4946insCGTGTGTGTGTG	XP_005264201.1:n.515-4947_515-4946insCGTGTGTGTGTG
XM_005264145.1:c.401-4947_401-4946insCGTGTGTGTGTG	XP_005264202.1:n.401-4947_401-4946insCGTGTGTGTGTG
XM_017003369.1:c.*521_*522insCGTGTGTGTGTG	XP_016858858.1:n.*521_*522insCGTGTGTGTGTG
XM_017003370.2:c.106+4877_106+4878insCGTGTGTGTGTG	XP_016858859.1:n.106+4877_106+4878insCGTGTGTGTGTG
XM_017003371.1:c.106+4877_106+4878insCGTGTGTGTGTG	XP_016858860.1:n.106+4877_106+4878insCGTGTGTGTGTG
XM_024452702.1:c.401-23166_401-23165insCGTGTGTGTGTG	XP_024308470.1:n.401-23166_401-23165insCGTGTGTGTGTG
XM_024452703.1:c.106+4877_106+4878insCGTGTGTGTGTG	XP_024308471.1:n.106+4877_106+4878insCGTGTGTGTGTG
XM_024452704.1:c.106+4877_106+4878insCGTGTGTGTGTG	XP_024308472.1:n.106+4877_106+4878insCGTGTGTGTGTG
XM_024452705.1:c.106+4877_106+4878insCGTGTGTGTGTG	XP_024308473.1:n.106+4877_106+4878insCGTGTGTGTGTG
NM_152390.3:c.652+4877_652+4878insCGTGTGTGTGTG MANE Select	NP_689603.2:n.652+4877_652+4878insCGTGTGTGTGTG
NM_001167959.2:c.106+4877_106+4878insCGTGTGTGTGTG	NP_001161431.1:n.106+4877_106+4878insCGTGTGTGTGTG