Canonical Allele Identifier: CA11041055
Gene: TMEFF2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10497721

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.192049636C>A , CM000664.2:g.192049636C>A GRCh38
NC_000002.11:g.192914362C>A , CM000664.1:g.192914362C>A GRCh37
NC_000002.10:g.192622607C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001305134.1:c.536+8043G>T VV NP_001292063.1:p.=
NM_016192.2:c.536+8043G>T VV NP_057276.2:p.=
NM_016192.3:c.536+8043G>T VV NP_057276.2:p.=
XM_005246437.2:c.536+8043G>T XP_005246494.1:p.=
XM_011510890.1:c.509+8043G>T XP_011509192.1:p.=
XR_923721.1:n.171+788C>A
XR_923722.1:n.171+788C>A
XM_011510890.3:c.509+8043G>T XP_011509192.1:p.=
XM_017003739.2:c.509+8043G>T XP_016859228.1:p.=
XM_017003740.2:c.536+8043G>T XP_016859229.1:p.=
XR_001739830.1:n.171+788C>A
NM_016192.4:c.536+8043G>T VV MANE Preferred NP_057276.2:p.=
ENST00000272771.9:c.536+8043G>T ENSP00000272771.5:p.=
ENST00000392314.5:c.536+8043G>T ENSP00000376128.1:p.=