Canonical Allele Identifier: CA2701286585

Gene: TMEFF2

Linked Data

• dbSNP Id: rs2105894958

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.192049697_192049715dup , CM000664.2:g.192049697_192049715dup	GRCh38
NC_000002.11:g.192914423_192914441dup , CM000664.1:g.192914423_192914441dup	GRCh37
NC_000002.10:g.192622668_192622686dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000272771.10:c.536+7973_536+7991dup MANE Select	ENSP00000272771.5:n.536+7973_536+7991dup
ENST00000272771.9:c.536+7973_536+7991dup	ENSP00000272771.5:n.536+7973_536+7991dup
ENST00000392314.5:c.536+7973_536+7991dup	ENSP00000376128.1:n.536+7973_536+7991dup
NM_001305134.1:c.536+7973_536+7991dup	NP_001292063.1:n.536+7973_536+7991dup
NM_016192.2:c.536+7973_536+7991dup	NP_057276.2:n.536+7973_536+7991dup
NM_016192.3:c.536+7973_536+7991dup	NP_057276.2:n.536+7973_536+7991dup
XM_005246437.2:c.536+7973_536+7991dup	XP_005246494.1:n.536+7973_536+7991dup
XM_011510890.1:c.509+7973_509+7991dup	XP_011509192.1:n.509+7973_509+7991dup
XR_923721.1:n.171+849_171+867dup
XR_923722.1:n.171+849_171+867dup
XM_011510890.3:c.509+7973_509+7991dup	XP_011509192.1:n.509+7973_509+7991dup
XM_017003739.2:c.509+7973_509+7991dup	XP_016859228.1:n.509+7973_509+7991dup
XM_017003740.2:c.536+7973_536+7991dup	XP_016859229.1:n.536+7973_536+7991dup
XR_001739830.1:n.171+849_171+867dup
NM_016192.4:c.536+7973_536+7991dup MANE Select	NP_057276.2:n.536+7973_536+7991dup
NM_001305134.2:c.536+7973_536+7991dup	NP_001292063.1:n.536+7973_536+7991dup