Canonical Allele Identifier: CA807137705

Gene: TENM2

Linked Data

• dbSNP Id: rs1405595681
• gnomAD v2: 5-166471201-CTG-C
• MyVariant Identifiers: chr5:g.166471202_166471203del (hg19) ; chr5:g.167044197_167044198del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044199_167044200del , CM000667.2:g.167044199_167044200del	GRCh38
NC_000005.9:g.166471204_166471205del , CM000667.1:g.166471204_166471205del	GRCh37
NC_000005.8:g.166403782_166403783del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29043_-189-29042del MANE Select	ENSP00000429430.1:n.-189-29043_-189-29042del
ENST00000695884.1:n.464-29043_464-29042del
XM_005265950.1:c.-189-29043_-189-29042del	XP_005266007.1:n.-189-29043_-189-29042del
XM_006714897.1:c.-189-29043_-189-29042del	XP_006714960.1:n.-189-29043_-189-29042del
XM_011534604.1:c.-189-29043_-189-29042del	XP_011532906.1:n.-189-29043_-189-29042del
XM_005265950.2:c.-189-29043_-189-29042del	XP_005266007.1:n.-189-29043_-189-29042del
XM_006714897.2:c.-189-29043_-189-29042del	XP_006714960.1:n.-189-29043_-189-29042del
XM_011534604.2:c.-189-29043_-189-29042del	XP_011532906.1:n.-189-29043_-189-29042del
XM_017009660.1:c.-189-29043_-189-29042del	XP_016865149.1:n.-189-29043_-189-29042del
XM_017009661.1:c.-189-29043_-189-29042del	XP_016865150.1:n.-189-29043_-189-29042del
XM_017009662.1:c.-189-29043_-189-29042del	XP_016865151.1:n.-189-29043_-189-29042del
NM_001395460.1:c.-189-29043_-189-29042del MANE Select	NP_001382389.1:n.-189-29043_-189-29042del