Canonical Allele Identifier: CA1246491551

Gene: TMEM178A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.39712537_39712538delinsAG , CM000664.2:g.39712537_39712538delinsAG	GRCh38
NC_000002.11:g.39939677_39939678delinsAG , CM000664.1:g.39939677_39939678delinsAG	GRCh37
NC_000002.10:g.39793181_39793182delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281961.3:c.653-4473_653-4472delinsAG MANE Select	ENSP00000281961.2:n.653-4473_653-4472delinsAG
ENST00000281961.2:c.653-4473_653-4472delinsAG	ENSP00000281961.2:n.653-4473_653-4472delinsAG
ENST00000413011.5:n.372-4473_372-4472delinsAG
ENST00000482239.5:n.396-4473_396-4472delinsAG
ENST00000495402.1:n.432-4473_432-4472delinsAG
ENST00000618232.1:c.*42-4473_*42-4472delinsAG	ENSP00000477622.1:n.*42-4473_*42-4472delinsAG
NM_001167959.1:c.107-4473_107-4472delinsAG	NP_001161431.1:n.107-4473_107-4472delinsAG
NM_152390.2:c.653-4473_653-4472delinsAG	NP_689603.2:n.653-4473_653-4472delinsAG
XM_005264144.1:c.515-4473_515-4472delinsAG	XP_005264201.1:n.515-4473_515-4472delinsAG
XM_005264145.1:c.401-4473_401-4472delinsAG	XP_005264202.1:n.401-4473_401-4472delinsAG
XM_017003369.1:c.*995_*996delinsAG	XP_016858858.1:n.*995_*996delinsAG
XM_017003370.2:c.107-4473_107-4472delinsAG	XP_016858859.1:n.107-4473_107-4472delinsAG
XM_017003371.1:c.107-4473_107-4472delinsAG	XP_016858860.1:n.107-4473_107-4472delinsAG
XM_024452702.1:c.401-22692_401-22691delinsAG	XP_024308470.1:n.401-22692_401-22691delinsAG
XM_024452703.1:c.107-4473_107-4472delinsAG	XP_024308471.1:n.107-4473_107-4472delinsAG
XM_024452704.1:c.107-4473_107-4472delinsAG	XP_024308472.1:n.107-4473_107-4472delinsAG
XM_024452705.1:c.107-4473_107-4472delinsAG	XP_024308473.1:n.107-4473_107-4472delinsAG
NM_152390.3:c.653-4473_653-4472delinsAG MANE Select	NP_689603.2:n.653-4473_653-4472delinsAG
NM_001167959.2:c.107-4473_107-4472delinsAG	NP_001161431.1:n.107-4473_107-4472delinsAG