Canonical Allele Identifier: CA1598775458
Gene: TENM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.167044065G= , CM000667.2:g.167044065G= GRCh38
NC_000005.9:g.166471070G= , CM000667.1:g.166471070G= GRCh37
NC_000005.8:g.166403648G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000518659.6:c.-189-29177G= MANE Select ENSP00000429430.1:n.-189-29177G=
ENST00000695884.1:n.464-29177G=
XM_005265950.1:c.-189-29177G= XP_005266007.1:n.-189-29177G=
XM_006714897.1:c.-189-29177G= XP_006714960.1:n.-189-29177G=
XM_011534604.1:c.-189-29177G= XP_011532906.1:n.-189-29177G=
XM_005265950.2:c.-189-29177G= XP_005266007.1:n.-189-29177G=
XM_006714897.2:c.-189-29177G= XP_006714960.1:n.-189-29177G=
XM_011534604.2:c.-189-29177G= XP_011532906.1:n.-189-29177G=
XM_017009660.1:c.-189-29177G= XP_016865149.1:n.-189-29177G=
XM_017009661.1:c.-189-29177G= XP_016865150.1:n.-189-29177G=
XM_017009662.1:c.-189-29177G= XP_016865151.1:n.-189-29177G=
NM_001395460.1:c.-189-29177G= MANE Select NP_001382389.1:n.-189-29177G=