Canonical Allele Identifier: CA807137361

Gene: TENM2

Linked Data

• dbSNP Id: rs1446373669
• gnomAD v3: 5-167044018-CAAAT-C
• gnomAD v4: 5-167044018-CAAAT-C
• MyVariant Identifiers: chr5:g.166471024_166471027del (hg19) ; chr5:g.167044019_167044022del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044024_167044027del , CM000667.2:g.167044024_167044027del	GRCh38
NC_000005.9:g.166471029_166471032del , CM000667.1:g.166471029_166471032del	GRCh37
NC_000005.8:g.166403607_166403610del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.-189-29218_-189-29215del MANE Select	ENSP00000429430.1:n.-189-29218_-189-29215del
ENST00000695884.1:n.464-29218_464-29215del
XM_005265950.1:c.-189-29218_-189-29215del	XP_005266007.1:n.-189-29218_-189-29215del
XM_006714897.1:c.-189-29218_-189-29215del	XP_006714960.1:n.-189-29218_-189-29215del
XM_011534604.1:c.-189-29218_-189-29215del	XP_011532906.1:n.-189-29218_-189-29215del
XM_005265950.2:c.-189-29218_-189-29215del	XP_005266007.1:n.-189-29218_-189-29215del
XM_006714897.2:c.-189-29218_-189-29215del	XP_006714960.1:n.-189-29218_-189-29215del
XM_011534604.2:c.-189-29218_-189-29215del	XP_011532906.1:n.-189-29218_-189-29215del
XM_017009660.1:c.-189-29218_-189-29215del	XP_016865149.1:n.-189-29218_-189-29215del
XM_017009661.1:c.-189-29218_-189-29215del	XP_016865150.1:n.-189-29218_-189-29215del
XM_017009662.1:c.-189-29218_-189-29215del	XP_016865151.1:n.-189-29218_-189-29215del
NM_001395460.1:c.-189-29218_-189-29215del MANE Select	NP_001382389.1:n.-189-29218_-189-29215del