Canonical Allele Identifier: CA807137660

Gene: TENM2

Linked Data

• dbSNP Id: rs1260917822
• gnomAD v3: 5-167044110-G-T
• gnomAD v4: 5-167044110-G-T
• MyVariant Identifiers: chr5:g.166471115G>T (hg19) ; chr5:g.167044110G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044110G>T , CM000667.2:g.167044110G>T	GRCh38
NC_000005.9:g.166471115G>T , CM000667.1:g.166471115G>T	GRCh37
NC_000005.8:g.166403693G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29132G>T MANE Select	ENSP00000429430.1:n.-189-29132G>T
ENST00000695884.1:n.464-29132G>T
XM_005265950.1:c.-189-29132G>T	XP_005266007.1:n.-189-29132G>T
XM_006714897.1:c.-189-29132G>T	XP_006714960.1:n.-189-29132G>T
XM_011534604.1:c.-189-29132G>T	XP_011532906.1:n.-189-29132G>T
XM_005265950.2:c.-189-29132G>T	XP_005266007.1:n.-189-29132G>T
XM_006714897.2:c.-189-29132G>T	XP_006714960.1:n.-189-29132G>T
XM_011534604.2:c.-189-29132G>T	XP_011532906.1:n.-189-29132G>T
XM_017009660.1:c.-189-29132G>T	XP_016865149.1:n.-189-29132G>T
XM_017009661.1:c.-189-29132G>T	XP_016865150.1:n.-189-29132G>T
XM_017009662.1:c.-189-29132G>T	XP_016865151.1:n.-189-29132G>T
NM_001395460.1:c.-189-29132G>T MANE Select	NP_001382389.1:n.-189-29132G>T