Canonical Allele Identifier: CA1598775488
Gene: TENM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.167044113C= , CM000667.2:g.167044113C= GRCh38
NC_000005.9:g.166471118C= , CM000667.1:g.166471118C= GRCh37
NC_000005.8:g.166403696C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518659.6:c.-189-29129C= MANE Select ENSP00000429430.1:n.-189-29129C=
ENST00000695884.1:n.464-29129C=
XM_005265950.1:c.-189-29129C= XP_005266007.1:n.-189-29129C=
XM_006714897.1:c.-189-29129C= XP_006714960.1:n.-189-29129C=
XM_011534604.1:c.-189-29129C= XP_011532906.1:n.-189-29129C=
XM_005265950.2:c.-189-29129C= XP_005266007.1:n.-189-29129C=
XM_006714897.2:c.-189-29129C= XP_006714960.1:n.-189-29129C=
XM_011534604.2:c.-189-29129C= XP_011532906.1:n.-189-29129C=
XM_017009660.1:c.-189-29129C= XP_016865149.1:n.-189-29129C=
XM_017009661.1:c.-189-29129C= XP_016865150.1:n.-189-29129C=
XM_017009662.1:c.-189-29129C= XP_016865151.1:n.-189-29129C=
NM_001395460.1:c.-189-29129C= MANE Select NP_001382389.1:n.-189-29129C=