Canonical Allele Identifier: CA1084059256
Gene: TENM2 HGNC NCBI

Linked Data

dbSNP Id: rs1186669900

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.167044063_167044064insTGAA , CM000667.2:g.167044063_167044064insTGAA GRCh38
NC_000005.9:g.166471068_166471069insTGAA , CM000667.1:g.166471068_166471069insTGAA GRCh37
NC_000005.8:g.166403646_166403647insTGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000518659.6:c.-189-29179_-189-29178insTGAA MANE Select ENSP00000429430.1:n.-189-29179_-189-29178insTGAA
ENST00000695884.1:n.464-29179_464-29178insTGAA
XM_005265950.1:c.-189-29179_-189-29178insTGAA XP_005266007.1:n.-189-29179_-189-29178insTGAA
XM_006714897.1:c.-189-29179_-189-29178insTGAA XP_006714960.1:n.-189-29179_-189-29178insTGAA
XM_011534604.1:c.-189-29179_-189-29178insTGAA XP_011532906.1:n.-189-29179_-189-29178insTGAA
XM_005265950.2:c.-189-29179_-189-29178insTGAA XP_005266007.1:n.-189-29179_-189-29178insTGAA
XM_006714897.2:c.-189-29179_-189-29178insTGAA XP_006714960.1:n.-189-29179_-189-29178insTGAA
XM_011534604.2:c.-189-29179_-189-29178insTGAA XP_011532906.1:n.-189-29179_-189-29178insTGAA
XM_017009660.1:c.-189-29179_-189-29178insTGAA XP_016865149.1:n.-189-29179_-189-29178insTGAA
XM_017009661.1:c.-189-29179_-189-29178insTGAA XP_016865150.1:n.-189-29179_-189-29178insTGAA
XM_017009662.1:c.-189-29179_-189-29178insTGAA XP_016865151.1:n.-189-29179_-189-29178insTGAA
NM_001395460.1:c.-189-29179_-189-29178insTGAA MANE Select NP_001382389.1:n.-189-29179_-189-29178insTGAA