Canonical Allele Identifier: CA1316747937

Gene: TMEFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.192050136_192050141delinsTATAAA , CM000664.2:g.192050136_192050141delinsTATAAA	GRCh38
NC_000002.11:g.192914862_192914867delinsTATAAA , CM000664.1:g.192914862_192914867delinsTATAAA	GRCh37
NC_000002.10:g.192623107_192623112delinsTATAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272771.10:c.536+7538_536+7543delinsTTTATA MANE Select	ENSP00000272771.5:n.536+7538_536+7543delinsTTTATA
ENST00000272771.9:c.536+7538_536+7543delinsTTTATA	ENSP00000272771.5:n.536+7538_536+7543delinsTTTATA
ENST00000392314.5:c.536+7538_536+7543delinsTTTATA	ENSP00000376128.1:n.536+7538_536+7543delinsTTTATA
NM_001305134.1:c.536+7538_536+7543delinsTTTATA	NP_001292063.1:n.536+7538_536+7543delinsTTTATA
NM_016192.2:c.536+7538_536+7543delinsTTTATA	NP_057276.2:n.536+7538_536+7543delinsTTTATA
NM_016192.3:c.536+7538_536+7543delinsTTTATA	NP_057276.2:n.536+7538_536+7543delinsTTTATA
XM_005246437.2:c.536+7538_536+7543delinsTTTATA	XP_005246494.1:n.536+7538_536+7543delinsTTTATA
XM_011510890.1:c.509+7538_509+7543delinsTTTATA	XP_011509192.1:n.509+7538_509+7543delinsTTTATA
XR_923721.1:n.172-468_172-463delinsTATAAA
XR_923722.1:n.172-468_172-463delinsTATAAA
XM_011510890.3:c.509+7538_509+7543delinsTTTATA	XP_011509192.1:n.509+7538_509+7543delinsTTTATA
XM_017003739.2:c.509+7538_509+7543delinsTTTATA	XP_016859228.1:n.509+7538_509+7543delinsTTTATA
XM_017003740.2:c.536+7538_536+7543delinsTTTATA	XP_016859229.1:n.536+7538_536+7543delinsTTTATA
XR_001739830.1:n.172-468_172-463delinsTATAAA
NM_016192.4:c.536+7538_536+7543delinsTTTATA MANE Select	NP_057276.2:n.536+7538_536+7543delinsTTTATA
NM_001305134.2:c.536+7538_536+7543delinsTTTATA	NP_001292063.1:n.536+7538_536+7543delinsTTTATA