Canonical Allele Identifier: CA11134413
Gene: TMEFF2 HGNC NCBI

Linked Data

dbSNP Id: rs13007495

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.192090779T>C , CM000664.2:g.192090779T>C GRCh38
NC_000002.11:g.192955505T>C , CM000664.1:g.192955505T>C GRCh37
NC_000002.10:g.192663750T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272771.10:c.440-33004A>G MANE Select ENSP00000272771.5:n.440-33004A>G
ENST00000272771.9:c.440-33004A>G ENSP00000272771.5:n.440-33004A>G
ENST00000392314.5:c.440-33004A>G ENSP00000376128.1:n.440-33004A>G
NM_001305134.1:c.440-33004A>G NP_001292063.1:n.440-33004A>G
NM_016192.2:c.440-33004A>G NP_057276.2:n.440-33004A>G
NM_016192.3:c.440-33004A>G NP_057276.2:n.440-33004A>G
XM_005246437.2:c.440-33004A>G XP_005246494.1:n.440-33004A>G
XM_011510890.1:c.413-33004A>G XP_011509192.1:n.413-33004A>G
XM_011510890.3:c.413-33004A>G XP_011509192.1:n.413-33004A>G
XM_017003739.2:c.413-33004A>G XP_016859228.1:n.413-33004A>G
XM_017003740.2:c.440-33004A>G XP_016859229.1:n.440-33004A>G
NM_016192.4:c.440-33004A>G MANE Select NP_057276.2:n.440-33004A>G
NM_001305134.2:c.440-33004A>G NP_001292063.1:n.440-33004A>G