Canonical Allele Identifier: CA10634340

Gene: TNNT3

Linked Data

• ClinVar Variation Id: 303964
• ClinVar RCV Id: RCV000352685 ; RCV000392505
• dbSNP Id: rs886048104
• gnomAD v2: 11-1940826-G-GC
• gnomAD v3: 11-1919596-G-GC
• gnomAD v4: 11-1919596-G-GC
• MyVariant Identifiers: chr11:g.1940834dupC (hg19) ; chr11:g.1940826_1940827insC (hg19) ; chr11:g.1919604dupC (hg38) ; chr11:g.1919596_1919597insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1919604dup , CM000673.2:g.1919604dup	GRCh38
NC_000011.9:g.1940834dup , CM000673.1:g.1940834dup	GRCh37
NC_000011.8:g.1897410dup	NCBI36
NG_013085.1:g.5036dup
NG_013085.2:g.5036dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278317.10:c.-177dup	ENSP00000278317.6:n.-177dup
NM_001042780.2:c.-177dup	NP_001036245.1:n.-177dup
NM_001042781.2:c.-177dup	NP_001036246.1:n.-177dup
NM_001042782.2:c.-177dup	NP_001036247.1:n.-177dup
NM_001297646.1:c.-435dup	NP_001284575.1:n.-435dup
NM_006757.3:c.-177dup	NP_006748.1:n.-177dup
XM_006718293.1:c.-177dup	XP_006718356.1:n.-177dup
XM_006718294.2:c.-177dup	XP_006718357.1:n.-177dup
XM_011520342.1:c.-177dup	XP_011518644.1:n.-177dup
NM_001363561.1:c.-177dup	NP_001350490.1:n.-177dup
XM_006718294.3:c.-177dup	XP_006718357.1:n.-177dup
XM_017018205.1:c.-177dup	XP_016873694.1:n.-177dup
XM_017018206.1:c.-19+31dup	XP_016873695.1:n.-19+31dup
XM_017018207.1:c.-19+31dup	XP_016873696.1:n.-19+31dup
XM_017018209.1:c.-19+31dup	XP_016873698.1:n.-19+31dup
XM_017018211.1:c.-19+31dup	XP_016873700.1:n.-19+31dup
XM_024448669.1:c.-19+31dup	XP_024304437.1:n.-19+31dup