Canonical Allele Identifier: CA1316747894

Gene: TMEFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.192050016_192050020delinsAAAAG , CM000664.2:g.192050016_192050020delinsAAAAG	GRCh38
NC_000002.11:g.192914742_192914746delinsAAAAG , CM000664.1:g.192914742_192914746delinsAAAAG	GRCh37
NC_000002.10:g.192622987_192622991delinsAAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272771.10:c.536+7659_536+7663delinsCTTTT MANE Select	ENSP00000272771.5:n.536+7659_536+7663delinsCTTTT
ENST00000272771.9:c.536+7659_536+7663delinsCTTTT	ENSP00000272771.5:n.536+7659_536+7663delinsCTTTT
ENST00000392314.5:c.536+7659_536+7663delinsCTTTT	ENSP00000376128.1:n.536+7659_536+7663delinsCTTTT
NM_001305134.1:c.536+7659_536+7663delinsCTTTT	NP_001292063.1:n.536+7659_536+7663delinsCTTTT
NM_016192.2:c.536+7659_536+7663delinsCTTTT	NP_057276.2:n.536+7659_536+7663delinsCTTTT
NM_016192.3:c.536+7659_536+7663delinsCTTTT	NP_057276.2:n.536+7659_536+7663delinsCTTTT
XM_005246437.2:c.536+7659_536+7663delinsCTTTT	XP_005246494.1:n.536+7659_536+7663delinsCTTTT
XM_011510890.1:c.509+7659_509+7663delinsCTTTT	XP_011509192.1:n.509+7659_509+7663delinsCTTTT
XR_923721.1:n.172-588_172-584delinsAAAAG
XR_923722.1:n.172-588_172-584delinsAAAAG
XM_011510890.3:c.509+7659_509+7663delinsCTTTT	XP_011509192.1:n.509+7659_509+7663delinsCTTTT
XM_017003739.2:c.509+7659_509+7663delinsCTTTT	XP_016859228.1:n.509+7659_509+7663delinsCTTTT
XM_017003740.2:c.536+7659_536+7663delinsCTTTT	XP_016859229.1:n.536+7659_536+7663delinsCTTTT
XR_001739830.1:n.172-588_172-584delinsAAAAG
NM_016192.4:c.536+7659_536+7663delinsCTTTT MANE Select	NP_057276.2:n.536+7659_536+7663delinsCTTTT
NM_001305134.2:c.536+7659_536+7663delinsCTTTT	NP_001292063.1:n.536+7659_536+7663delinsCTTTT