Canonical Allele Identifier: CA131694671

Gene: TENM2

Linked Data

• dbSNP Id: rs773879068
• gnomAD v2: 5-166471114-G-A
• gnomAD v3: 5-167044109-G-A
• gnomAD v4: 5-167044109-G-A
• MyVariant Identifiers: chr5:g.166471114G>A (hg19) ; chr5:g.167044109G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044109G>A , CM000667.2:g.167044109G>A	GRCh38
NC_000005.9:g.166471114G>A , CM000667.1:g.166471114G>A	GRCh37
NC_000005.8:g.166403692G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29133G>A MANE Select	ENSP00000429430.1:n.-189-29133G>A
ENST00000695884.1:n.464-29133G>A
XM_005265950.1:c.-189-29133G>A	XP_005266007.1:n.-189-29133G>A
XM_006714897.1:c.-189-29133G>A	XP_006714960.1:n.-189-29133G>A
XM_011534604.1:c.-189-29133G>A	XP_011532906.1:n.-189-29133G>A
XM_005265950.2:c.-189-29133G>A	XP_005266007.1:n.-189-29133G>A
XM_006714897.2:c.-189-29133G>A	XP_006714960.1:n.-189-29133G>A
XM_011534604.2:c.-189-29133G>A	XP_011532906.1:n.-189-29133G>A
XM_017009660.1:c.-189-29133G>A	XP_016865149.1:n.-189-29133G>A
XM_017009661.1:c.-189-29133G>A	XP_016865150.1:n.-189-29133G>A
XM_017009662.1:c.-189-29133G>A	XP_016865151.1:n.-189-29133G>A
NM_001395460.1:c.-189-29133G>A MANE Select	NP_001382389.1:n.-189-29133G>A