Canonical Allele Identifier: CA10654653

Gene: TSEN2

Linked Data

• ClinVar Variation Id: 369384
• ClinVar RCV Id: RCV000302493 ; RCV001709646
• dbSNP Id: rs3806662
• gnomAD v2: 3-12526006-G-A
• gnomAD v3: 3-12484507-G-A
• gnomAD v4: 3-12484507-G-A
• MyVariant Identifiers: chr3:g.12526006G>A (hg19) ; chr3:g.12484507G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12484507G>A , CM000665.2:g.12484507G>A	GRCh38
NC_000003.11:g.12526006G>A , CM000665.1:g.12526006G>A	GRCh37
NC_000003.10:g.12501006G>A	NCBI36
NG_011521.1:g.5076G>A
NG_011521.2:g.5076G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284995.11:c.-391G>A MANE Select	ENSP00000284995.6:n.-391G>A
ENST00000412698.3:c.-28G>A	ENSP00000408528.3:n.-28G>A
ENST00000415684.6:c.-28G>A	ENSP00000416510.1:n.-28G>A
ENST00000446004.6:c.-28G>A	ENSP00000406238.2:n.-28G>A
ENST00000455118.6:c.-28G>A	ENSP00000408744.2:n.-28G>A
ENST00000475595.2:n.73G>A
ENST00000679424.1:c.-28G>A	ENSP00000505917.1:n.-28G>A
ENST00000679537.1:n.73G>A
ENST00000679670.1:c.-28G>A	ENSP00000506080.1:n.-28G>A
ENST00000679699.1:c.-28G>A	ENSP00000505274.1:n.-28G>A
ENST00000679756.1:c.-28G>A	ENSP00000506391.1:n.-28G>A
ENST00000679995.1:c.-1332G>A	ENSP00000505221.1:n.-1332G>A
ENST00000680126.1:c.-28G>A	ENSP00000505345.1:n.-28G>A
ENST00000680275.1:c.-28G>A	ENSP00000505417.1:n.-28G>A
ENST00000680376.1:c.-28G>A	ENSP00000506369.1:n.-28G>A
ENST00000680458.1:c.-28G>A	ENSP00000505979.1:n.-28G>A
ENST00000680765.1:c.-28G>A	ENSP00000505351.1:n.-28G>A
ENST00000680817.1:c.-28G>A	ENSP00000506221.1:n.-28G>A
ENST00000680873.1:c.-28G>A	ENSP00000505233.1:n.-28G>A
ENST00000680923.1:c.-28G>A	ENSP00000505344.1:n.-28G>A
ENST00000681073.1:c.-28G>A	ENSP00000506576.1:n.-28G>A
ENST00000681343.1:c.-28G>A	ENSP00000506265.1:n.-28G>A
ENST00000681433.1:c.-28G>A	ENSP00000505729.1:n.-28G>A
ENST00000681482.1:c.-28G>A	ENSP00000505436.1:n.-28G>A
ENST00000681676.1:c.-391G>A	ENSP00000506163.1:n.-391G>A
ENST00000681713.1:c.-28G>A	ENSP00000506046.1:n.-28G>A
ENST00000402228.7:c.-139G>A	ENSP00000385976.3:n.-139G>A
ENST00000446004.5:c.-28G>A	ENSP00000406238.1:n.-28G>A
ENST00000454502.6:c.-28G>A	ENSP00000392029.2:n.-28G>A
NM_001145393.1:c.-28G>A	NP_001138865.1:n.-28G>A
NM_001145394.1:c.-28G>A	NP_001138866.1:n.-28G>A
XM_005265495.1:c.-28G>A	XP_005265552.1:n.-28G>A
XM_005265498.1:c.-28G>A	XP_005265555.1:n.-28G>A
XM_005265499.2:c.-28G>A	XP_005265556.1:n.-28G>A
XM_011534140.1:c.-28G>A	XP_011532442.1:n.-28G>A
XR_245158.1:n.76G>A
XR_245159.3:n.76G>A
XR_427296.1:n.76G>A
XR_940503.1:n.76G>A
NM_001145393.2:c.-28G>A	NP_001138865.1:n.-28G>A
NM_001321277.1:c.-28G>A	NP_001308206.1:n.-28G>A
NM_001321278.1:c.-28G>A	NP_001308207.1:n.-28G>A
NR_135607.1:n.76G>A
XM_017007292.1:c.-28G>A	XP_016862781.1:n.-28G>A
XM_024453785.1:c.-139G>A	XP_024309553.1:n.-139G>A
XR_001740290.2:n.52G>A
XR_001740294.2:n.52G>A
XR_001740295.2:n.52G>A
XR_001740298.2:n.52G>A
XR_001740300.2:n.52G>A
XR_001740301.2:n.52G>A
XR_001740302.2:n.52G>A
XR_001740303.2:n.52G>A
XR_002959594.1:n.52G>A
XR_427296.2:n.52G>A
NM_001321278.2:c.-28G>A	NP_001308207.1:n.-28G>A
NM_025265.4:c.-391G>A MANE Select	NP_079541.1:n.-391G>A
NR_135607.2:n.28G>A
NM_001145392.2:c.-139G>A	NP_001138864.1:n.-139G>A
NM_001145393.3:c.-28G>A	NP_001138865.1:n.-28G>A
NM_001145394.2:c.-28G>A	NP_001138866.1:n.-28G>A
NM_001321277.2:c.-28G>A	NP_001308206.1:n.-28G>A
NM_001321279.2:c.-391G>A	NP_001308208.1:n.-391G>A