Canonical Allele Identifier: CA11988280
Gene: TENM2 HGNC NCBI

Linked Data

dbSNP Id: rs2937573
gnomAD v2: 5-166471198-G-A
gnomAD v3: 5-167044193-G-A
gnomAD v4: 5-167044193-G-A
MyVariant Identifiers: chr5:g.166471198G>A (hg19) chr5:g.167044193G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.167044193G>A , CM000667.2:g.167044193G>A GRCh38
NC_000005.9:g.166471198G>A , CM000667.1:g.166471198G>A GRCh37
NC_000005.8:g.166403776G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518659.6:c.-189-29049G>A MANE Select ENSP00000429430.1:n.-189-29049G>A
ENST00000695884.1:n.464-29049G>A
XM_005265950.1:c.-189-29049G>A XP_005266007.1:n.-189-29049G>A
XM_006714897.1:c.-189-29049G>A XP_006714960.1:n.-189-29049G>A
XM_011534604.1:c.-189-29049G>A XP_011532906.1:n.-189-29049G>A
XM_005265950.2:c.-189-29049G>A XP_005266007.1:n.-189-29049G>A
XM_006714897.2:c.-189-29049G>A XP_006714960.1:n.-189-29049G>A
XM_011534604.2:c.-189-29049G>A XP_011532906.1:n.-189-29049G>A
XM_017009660.1:c.-189-29049G>A XP_016865149.1:n.-189-29049G>A
XM_017009661.1:c.-189-29049G>A XP_016865150.1:n.-189-29049G>A
XM_017009662.1:c.-189-29049G>A XP_016865151.1:n.-189-29049G>A
NM_001395460.1:c.-189-29049G>A MANE Select NP_001382389.1:n.-189-29049G>A
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