Canonical Allele Identifier: CA1246491427

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712231_39712232delinsGA , CM000664.2:g.39712231_39712232delinsGA	GRCh38
NC_000002.11:g.39939371_39939372delinsGA , CM000664.1:g.39939371_39939372delinsGA	GRCh37
NC_000002.10:g.39792875_39792876delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.653-4779_653-4778delinsGA MANE Select	ENSP00000281961.2:n.653-4779_653-4778delinsGA
ENST00000281961.2:c.653-4779_653-4778delinsGA	ENSP00000281961.2:n.653-4779_653-4778delinsGA
ENST00000413011.5:n.372-4779_372-4778delinsGA
ENST00000482239.5:n.396-4779_396-4778delinsGA
ENST00000495402.1:n.432-4779_432-4778delinsGA
ENST00000618232.1:c.*42-4779_*42-4778delinsGA	ENSP00000477622.1:n.*42-4779_*42-4778delinsGA
NM_001167959.1:c.107-4779_107-4778delinsGA	NP_001161431.1:n.107-4779_107-4778delinsGA
NM_152390.2:c.653-4779_653-4778delinsGA	NP_689603.2:n.653-4779_653-4778delinsGA
XM_005264144.1:c.515-4779_515-4778delinsGA	XP_005264201.1:n.515-4779_515-4778delinsGA
XM_005264145.1:c.401-4779_401-4778delinsGA	XP_005264202.1:n.401-4779_401-4778delinsGA
XM_017003369.1:c.*689_*690delinsGA	XP_016858858.1:n.*689_*690delinsGA
XM_017003370.2:c.107-4779_107-4778delinsGA	XP_016858859.1:n.107-4779_107-4778delinsGA
XM_017003371.1:c.107-4779_107-4778delinsGA	XP_016858860.1:n.107-4779_107-4778delinsGA
XM_024452702.1:c.401-22998_401-22997delinsGA	XP_024308470.1:n.401-22998_401-22997delinsGA
XM_024452703.1:c.107-4779_107-4778delinsGA	XP_024308471.1:n.107-4779_107-4778delinsGA
XM_024452704.1:c.107-4779_107-4778delinsGA	XP_024308472.1:n.107-4779_107-4778delinsGA
XM_024452705.1:c.107-4779_107-4778delinsGA	XP_024308473.1:n.107-4779_107-4778delinsGA
NM_152390.3:c.653-4779_653-4778delinsGA MANE Select	NP_689603.2:n.653-4779_653-4778delinsGA
NM_001167959.2:c.107-4779_107-4778delinsGA	NP_001161431.1:n.107-4779_107-4778delinsGA