Canonical Allele Identifier: CA564379538

Gene: TENM2

Linked Data

• dbSNP Id: rs1281400472
• gnomAD v2: 5-166471022-T-C
• gnomAD v3: 5-167044017-T-C
• gnomAD v4: 5-167044017-T-C
• MyVariant Identifiers: chr5:g.166471022T>C (hg19) ; chr5:g.167044017T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044017T>C , CM000667.2:g.167044017T>C	GRCh38
NC_000005.9:g.166471022T>C , CM000667.1:g.166471022T>C	GRCh37
NC_000005.8:g.166403600T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29225T>C MANE Select	ENSP00000429430.1:n.-189-29225T>C
ENST00000695884.1:n.464-29225T>C
XM_005265950.1:c.-189-29225T>C	XP_005266007.1:n.-189-29225T>C
XM_006714897.1:c.-189-29225T>C	XP_006714960.1:n.-189-29225T>C
XM_011534604.1:c.-189-29225T>C	XP_011532906.1:n.-189-29225T>C
XM_005265950.2:c.-189-29225T>C	XP_005266007.1:n.-189-29225T>C
XM_006714897.2:c.-189-29225T>C	XP_006714960.1:n.-189-29225T>C
XM_011534604.2:c.-189-29225T>C	XP_011532906.1:n.-189-29225T>C
XM_017009660.1:c.-189-29225T>C	XP_016865149.1:n.-189-29225T>C
XM_017009661.1:c.-189-29225T>C	XP_016865150.1:n.-189-29225T>C
XM_017009662.1:c.-189-29225T>C	XP_016865151.1:n.-189-29225T>C
NM_001395460.1:c.-189-29225T>C MANE Select	NP_001382389.1:n.-189-29225T>C