Canonical Allele Identifier: CA351443324

Gene: TRNT1

Linked Data

• ClinVar Variation Id: 2113353
• ClinVar RCV Id: RCV003027278
• MyVariant Identifiers: chr3:g.3179130C>G (hg19) ; chr3:g.3137446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3137446C>G , CM000665.2:g.3137446C>G	GRCh38
NC_000003.11:g.3179130C>G , CM000665.1:g.3179130C>G	GRCh37
NC_000003.10:g.3154130C>G	NCBI36
NG_041800.1:g.15531C>G
NG_041800.2:g.15531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698406.1:c.335C>G	ENSP00000513700.1:p.Thr112Ser
ENST00000698407.1:n.964C>G
ENST00000698408.1:c.335C>G	ENSP00000513701.1:p.Thr112Ser
ENST00000698409.1:n.402C>G
ENST00000698410.1:c.335C>G	ENSP00000513703.1:p.Thr112Ser
ENST00000698412.1:c.335C>G	ENSP00000513705.1:p.Thr112Ser
ENST00000698413.1:c.452C>G	ENSP00000513706.1:p.Thr151Ser
ENST00000698414.1:c.452C>G	ENSP00000513707.1:p.Thr151Ser
ENST00000698415.1:n.1696C>G
ENST00000251607.11:c.335C>G MANE Select	ENSP00000251607.6:p.Thr112Ser
ENST00000397779.3:c.335C>G	ENSP00000380881.3:p.Thr112Ser
ENST00000650755.1:c.149-3064C>G	ENSP00000499122.1:n.149-3064C>G
ENST00000650814.1:c.91C>G
ENST00000650839.1:c.335C>G	ENSP00000498970.1:p.Thr112Ser
ENST00000650989.1:n.215C>G
ENST00000651093.1:c.335C>G	ENSP00000498942.1:p.Thr112Ser
ENST00000651316.1:c.335C>G	ENSP00000498787.1:p.Thr112Ser
ENST00000651352.1:c.335C>G	ENSP00000498449.1:p.Thr112Ser
ENST00000651591.1:c.*259C>G	ENSP00000498240.1:n.*259C>G
ENST00000251607.10:c.335C>G	ENSP00000251607.6:p.Thr112Ser
ENST00000280591.10:c.335C>G	ENSP00000280591.6:p.Thr112Ser
ENST00000434583.5:c.335C>G	ENSP00000415100.1:p.Thr112Ser
ENST00000482311.1:n.221C>G
NM_001302946.1:c.335C>G	NP_001289875.1:p.Thr112Ser
NM_182916.2:c.335C>G	NP_886552.2:p.Thr112Ser
XM_005265196.1:c.335C>G	XP_005265253.1:p.Thr112Ser
XM_011533776.1:c.335C>G	XP_011532078.1:p.Thr112Ser
XM_011533777.1:c.335C>G	XP_011532079.1:p.Thr112Ser
XM_011533778.1:c.335C>G	XP_011532080.1:p.Thr112Ser
XR_940445.1:n.437C>G
XR_940446.1:n.437C>G
XM_011533776.3:c.335C>G	XP_011532078.1:p.Thr112Ser
XM_011533777.2:c.335C>G	XP_011532079.1:p.Thr112Ser
XM_011533778.3:c.335C>G	XP_011532080.1:p.Thr112Ser
XR_001740168.2:n.416C>G
XR_001740169.2:n.416C>G
XR_940445.3:n.416C>G
XR_940446.3:n.416C>G
NM_001302946.2:c.335C>G	NP_001289875.2:p.Thr112Ser
NM_001367321.1:c.335C>G	NP_001354250.1:p.Thr112Ser
NM_001367322.1:c.335C>G	NP_001354251.1:p.Thr112Ser
NM_001367323.1:c.335C>G	NP_001354252.1:p.Thr112Ser
NM_182916.3:c.335C>G MANE Select	NP_886552.3:p.Thr112Ser
NR_159934.1:n.413C>G
NR_159935.1:n.413C>G
NR_159936.1:n.413C>G
NR_159937.1:n.1441C>G
NR_159938.1:n.413C>G
NR_159939.1:n.413C>G
NR_159940.1:n.413C>G
NR_159941.1:n.1441C>G