Canonical Allele Identifier: CA10581123
Gene: TRNT1 HGNC NCBI
CRBN HGNC NCBI

Linked Data

ClinVar Variation Id: 234935
ClinVar RCV Id: RCV000223676 RCV001854766
dbSNP Id: rs876661299
gnomAD v2: 3-3188088-T-C
gnomAD v4: 3-3146404-T-C
MyVariant Identifiers: chr3:g.3188088T>C (hg19) chr3:g.3146404T>C (hg38)
PubMed: PMID:26494905
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.3146404T>C , CM000665.2:g.3146404T>C GRCh38
NC_000003.11:g.3188088T>C , CM000665.1:g.3188088T>C GRCh37
NC_000003.10:g.3163088T>C NCBI36
NG_041800.1:g.24489T>C
NG_041800.2:g.24489T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698406.1:c.609-26T>C (TRNT1) ENSP00000513700.1:n.609-26T>C
ENST00000698407.1:n.1238-26T>C (TRNT1)
ENST00000698408.1:c.609-26T>C (TRNT1) ENSP00000513701.1:n.609-26T>C
ENST00000698410.1:c.*80-26T>C (TRNT1) ENSP00000513703.1:n.*80-26T>C
ENST00000698412.1:c.609-26T>C (TRNT1) ENSP00000513705.1:n.609-26T>C
ENST00000698413.1:c.726-26T>C (TRNT1) ENSP00000513706.1:n.726-26T>C
ENST00000698414.1:c.726-26T>C (TRNT1) ENSP00000513707.1:n.726-26T>C
ENST00000698415.1:n.1970-26T>C (TRNT1)
ENST00000698416.1:n.847T>C (TRNT1)
ENST00000251607.11:c.609-26T>C (TRNT1) MANE Select ENSP00000251607.6:n.609-26T>C
ENST00000639284.1:c.1312-905A>G (CRBN) ENSP00000491442.1:n.1312-905A>G
ENST00000650755.1:c.*259-26T>C (TRNT1) ENSP00000499122.1:n.*259-26T>C
ENST00000650814.1:c.295-12T>C (TRNT1)
ENST00000650839.1:c.609-12T>C (TRNT1) ENSP00000498970.1:n.609-12T>C
ENST00000650989.1:n.350-1046T>C (TRNT1)
ENST00000651093.1:c.609-1046T>C (TRNT1) ENSP00000498942.1:n.609-1046T>C
ENST00000651316.1:c.*148-1046T>C (TRNT1) ENSP00000498787.1:n.*148-1046T>C
ENST00000651352.1:c.*80-26T>C (TRNT1) ENSP00000498449.1:n.*80-26T>C
ENST00000651591.1:c.*533-1046T>C (TRNT1) ENSP00000498240.1:n.*533-1046T>C
ENST00000652340.1:c.402-26T>C (TRNT1) ENSP00000498624.1:n.402-26T>C
ENST00000251607.10:c.609-26T>C (TRNT1) ENSP00000251607.6:n.609-26T>C
ENST00000280591.10:c.609-26T>C (TRNT1) ENSP00000280591.6:n.609-26T>C
ENST00000434583.5:c.609-26T>C (TRNT1) ENSP00000415100.1:n.609-26T>C
NM_001302946.1:c.609-26T>C (TRNT1) NP_001289875.1:n.609-26T>C
NM_182916.2:c.609-26T>C (TRNT1) NP_886552.2:n.609-26T>C
XM_005265196.1:c.609-26T>C (TRNT1) XP_005265253.1:n.609-26T>C
XM_011533776.1:c.609-26T>C (TRNT1) XP_011532078.1:n.609-26T>C
XM_011533777.1:c.609-26T>C (TRNT1) XP_011532079.1:n.609-26T>C
XM_011533778.1:c.609-26T>C (TRNT1) XP_011532080.1:n.609-26T>C
XR_940445.1:n.711-26T>C (TRNT1)
XR_940446.1:n.711-26T>C (TRNT1)
XM_011533776.3:c.609-26T>C (TRNT1) XP_011532078.1:n.609-26T>C
XM_011533777.2:c.609-26T>C (TRNT1) XP_011532079.1:n.609-26T>C
XM_011533778.3:c.609-26T>C (TRNT1) XP_011532080.1:n.609-26T>C
XR_001740168.2:n.690-26T>C (TRNT1)
XR_001740169.2:n.690-26T>C (TRNT1)
XR_940445.3:n.690-26T>C (TRNT1)
XR_940446.3:n.690-26T>C (TRNT1)
NM_001302946.2:c.609-26T>C (TRNT1) NP_001289875.2:n.609-26T>C
NM_001367321.1:c.609-26T>C (TRNT1) NP_001354250.1:n.609-26T>C
NM_001367322.1:c.609-26T>C (TRNT1) NP_001354251.1:n.609-26T>C
NM_001367323.1:c.609-26T>C (TRNT1) NP_001354252.1:n.609-26T>C
NM_182916.3:c.609-26T>C (TRNT1) MANE Select NP_886552.3:n.609-26T>C
NR_159934.1:n.687-26T>C (TRNT1)
NR_159935.1:n.687-26T>C (TRNT1)
NR_159936.1:n.687-1046T>C (TRNT1)
NR_159937.1:n.1715-12T>C (TRNT1)
NR_159938.1:n.687-1046T>C (TRNT1)
NR_159939.1:n.548-26T>C (TRNT1)
NR_159940.1:n.548-12T>C (TRNT1)
NR_159941.1:n.1715-12T>C (TRNT1)
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