Canonical Allele Identifier: CA1598775463

Gene: TENM2

Linked Data

• dbSNP Id: rs1758183988

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044072_167044073insCAAG , CM000667.2:g.167044072_167044073insCAAG	GRCh38
NC_000005.9:g.166471077_166471078insCAAG , CM000667.1:g.166471077_166471078insCAAG	GRCh37
NC_000005.8:g.166403655_166403656insCAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.-189-29170_-189-29169insCAAG MANE Select	ENSP00000429430.1:n.-189-29170_-189-29169insCAAG
ENST00000695884.1:n.464-29170_464-29169insCAAG
XM_005265950.1:c.-189-29170_-189-29169insCAAG	XP_005266007.1:n.-189-29170_-189-29169insCAAG
XM_006714897.1:c.-189-29170_-189-29169insCAAG	XP_006714960.1:n.-189-29170_-189-29169insCAAG
XM_011534604.1:c.-189-29170_-189-29169insCAAG	XP_011532906.1:n.-189-29170_-189-29169insCAAG
XM_005265950.2:c.-189-29170_-189-29169insCAAG	XP_005266007.1:n.-189-29170_-189-29169insCAAG
XM_006714897.2:c.-189-29170_-189-29169insCAAG	XP_006714960.1:n.-189-29170_-189-29169insCAAG
XM_011534604.2:c.-189-29170_-189-29169insCAAG	XP_011532906.1:n.-189-29170_-189-29169insCAAG
XM_017009660.1:c.-189-29170_-189-29169insCAAG	XP_016865149.1:n.-189-29170_-189-29169insCAAG
XM_017009661.1:c.-189-29170_-189-29169insCAAG	XP_016865150.1:n.-189-29170_-189-29169insCAAG
XM_017009662.1:c.-189-29170_-189-29169insCAAG	XP_016865151.1:n.-189-29170_-189-29169insCAAG
NM_001395460.1:c.-189-29170_-189-29169insCAAG MANE Select	NP_001382389.1:n.-189-29170_-189-29169insCAAG