Canonical Allele Identifier: CA807137402

Gene: TENM2

Linked Data

• dbSNP Id: rs1291809266
• gnomAD v3: 5-167044026-TAGTAAGGACAGAAGGAAGGAAGGAAGGA-T
• gnomAD v4: 5-167044026-TAGTAAGGACAGAAGGAAGGAAGGAAGGA-T
• MyVariant Identifiers: chr5:g.166471032_166471059del (hg19) ; chr5:g.167044027_167044054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044029_167044056del , CM000667.2:g.167044029_167044056del	GRCh38
NC_000005.9:g.166471034_166471061del , CM000667.1:g.166471034_166471061del	GRCh37
NC_000005.8:g.166403612_166403639del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.-189-29213_-189-29186del MANE Select	ENSP00000429430.1:n.-189-29213_-189-29186del
ENST00000695884.1:n.464-29213_464-29186del
XM_005265950.1:c.-189-29213_-189-29186del	XP_005266007.1:n.-189-29213_-189-29186del
XM_006714897.1:c.-189-29213_-189-29186del	XP_006714960.1:n.-189-29213_-189-29186del
XM_011534604.1:c.-189-29213_-189-29186del	XP_011532906.1:n.-189-29213_-189-29186del
XM_005265950.2:c.-189-29213_-189-29186del	XP_005266007.1:n.-189-29213_-189-29186del
XM_006714897.2:c.-189-29213_-189-29186del	XP_006714960.1:n.-189-29213_-189-29186del
XM_011534604.2:c.-189-29213_-189-29186del	XP_011532906.1:n.-189-29213_-189-29186del
XM_017009660.1:c.-189-29213_-189-29186del	XP_016865149.1:n.-189-29213_-189-29186del
XM_017009661.1:c.-189-29213_-189-29186del	XP_016865150.1:n.-189-29213_-189-29186del
XM_017009662.1:c.-189-29213_-189-29186del	XP_016865151.1:n.-189-29213_-189-29186del
NM_001395460.1:c.-189-29213_-189-29186del MANE Select	NP_001382389.1:n.-189-29213_-189-29186del