Canonical Allele Identifier: CA131694677

Gene: TENM2

Linked Data

• dbSNP Id: rs192170664
• gnomAD v2: 5-166471157-A-G
• gnomAD v3: 5-167044152-A-G
• gnomAD v4: 5-167044152-A-G
• MyVariant Identifiers: chr5:g.166471157A>G (hg19) ; chr5:g.167044152A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044152A>G , CM000667.2:g.167044152A>G	GRCh38
NC_000005.9:g.166471157A>G , CM000667.1:g.166471157A>G	GRCh37
NC_000005.8:g.166403735A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29090A>G MANE Select	ENSP00000429430.1:n.-189-29090A>G
ENST00000695884.1:n.464-29090A>G
XM_005265950.1:c.-189-29090A>G	XP_005266007.1:n.-189-29090A>G
XM_006714897.1:c.-189-29090A>G	XP_006714960.1:n.-189-29090A>G
XM_011534604.1:c.-189-29090A>G	XP_011532906.1:n.-189-29090A>G
XM_005265950.2:c.-189-29090A>G	XP_005266007.1:n.-189-29090A>G
XM_006714897.2:c.-189-29090A>G	XP_006714960.1:n.-189-29090A>G
XM_011534604.2:c.-189-29090A>G	XP_011532906.1:n.-189-29090A>G
XM_017009660.1:c.-189-29090A>G	XP_016865149.1:n.-189-29090A>G
XM_017009661.1:c.-189-29090A>G	XP_016865150.1:n.-189-29090A>G
XM_017009662.1:c.-189-29090A>G	XP_016865151.1:n.-189-29090A>G
NM_001395460.1:c.-189-29090A>G MANE Select	NP_001382389.1:n.-189-29090A>G