Canonical Allele Identifier: CA16407355

Gene: TNNT3

Linked Data

• dbSNP Id: rs909116
• gnomAD v2: 11-1941946-T-C
• gnomAD v3: 11-1920716-T-C
• gnomAD v4: 11-1920716-T-C
• MyVariant Identifiers: chr11:g.1941946T>C (hg19) ; chr11:g.1920716T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1920716T>C , CM000673.2:g.1920716T>C	GRCh38
NC_000011.9:g.1941946T>C , CM000673.1:g.1941946T>C	GRCh37
NC_000011.8:g.1898522T>C	NCBI36
NG_013085.1:g.6148T>C
NG_013085.2:g.6148T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278317.11:c.-19+954T>C MANE Select	ENSP00000278317.6:n.-19+954T>C
ENST00000381558.6:c.-276-646T>C	ENSP00000370970.1:n.-276-646T>C
ENST00000278317.10:c.-19+954T>C	ENSP00000278317.6:n.-19+954T>C
ENST00000344578.8:c.-19+954T>C	ENSP00000344870.4:n.-19+954T>C
ENST00000381557.6:c.-19+954T>C	ENSP00000370969.2:n.-19+954T>C
ENST00000381563.8:c.-19+954T>C	ENSP00000370975.4:n.-19+954T>C
ENST00000381579.7:c.-19+954T>C	ENSP00000370991.3:n.-19+954T>C
ENST00000381589.7:c.-19+954T>C	ENSP00000371001.3:n.-19+954T>C
ENST00000453458.5:c.-19+954T>C	ENSP00000415614.1:n.-19+954T>C
NM_001042780.2:c.-19+954T>C	NP_001036245.1:n.-19+954T>C
NM_001042781.2:c.-19+954T>C	NP_001036246.1:n.-19+954T>C
NM_001042782.2:c.-19+954T>C	NP_001036247.1:n.-19+954T>C
NM_001297646.1:c.-276-646T>C	NP_001284575.1:n.-276-646T>C
NM_006757.3:c.-19+954T>C	NP_006748.1:n.-19+954T>C
XM_006718290.2:c.-19+954T>C	XP_006718353.1:n.-19+954T>C
XM_006718291.2:c.-19+954T>C	XP_006718354.1:n.-19+954T>C
XM_006718292.2:c.-19+954T>C	XP_006718355.1:n.-19+954T>C
XM_006718293.1:c.-19+954T>C	XP_006718356.1:n.-19+954T>C
XM_006718294.2:c.-19+954T>C	XP_006718357.1:n.-19+954T>C
XM_006718295.2:c.-19+954T>C	XP_006718358.1:n.-19+954T>C
XM_006718296.2:c.-19+954T>C	XP_006718359.1:n.-19+954T>C
XM_006718297.2:c.-19+954T>C	XP_006718360.1:n.-19+954T>C
XM_006718298.2:c.-19+954T>C	XP_006718361.1:n.-19+954T>C
XM_006718299.1:c.-19+954T>C	XP_006718362.1:n.-19+954T>C
XM_006718300.2:c.-19+954T>C	XP_006718363.1:n.-19+954T>C
XM_006718301.2:c.-19+954T>C	XP_006718364.1:n.-19+954T>C
XM_006718302.2:c.-19+954T>C	XP_006718365.1:n.-19+954T>C
XM_011520342.1:c.-19+954T>C	XP_011518644.1:n.-19+954T>C
NM_001363561.1:c.-19+954T>C	NP_001350490.1:n.-19+954T>C
XM_006718290.3:c.-19+954T>C	XP_006718353.1:n.-19+954T>C
XM_006718294.3:c.-19+954T>C	XP_006718357.1:n.-19+954T>C
XM_006718296.3:c.-19+954T>C	XP_006718359.1:n.-19+954T>C
XM_006718299.2:c.-19+954T>C	XP_006718362.1:n.-19+954T>C
XM_006718300.3:c.-19+954T>C	XP_006718363.1:n.-19+954T>C
XM_006718302.3:c.-19+954T>C	XP_006718365.1:n.-19+954T>C
XM_017018205.1:c.-19+954T>C	XP_016873694.1:n.-19+954T>C
XM_017018206.1:c.-19+1143T>C	XP_016873695.1:n.-19+1143T>C
XM_017018207.1:c.-19+1143T>C	XP_016873696.1:n.-19+1143T>C
XM_017018209.1:c.-19+1143T>C	XP_016873698.1:n.-19+1143T>C
XM_017018211.1:c.-19+1143T>C	XP_016873700.1:n.-19+1143T>C
XM_017018216.1:c.-19+954T>C	XP_016873705.1:n.-19+954T>C
XM_017018217.1:c.-19+954T>C	XP_016873706.1:n.-19+954T>C
XM_017018218.1:c.-19+954T>C	XP_016873707.1:n.-19+954T>C
XM_017018219.1:c.-19+954T>C	XP_016873708.1:n.-19+954T>C
XM_024448669.1:c.-19+1143T>C	XP_024304437.1:n.-19+1143T>C
NM_001367845.1:c.-19+954T>C	NP_001354774.1:n.-19+954T>C
NM_001367846.1:c.-19+954T>C	NP_001354775.1:n.-19+954T>C
NM_001367848.1:c.-19+954T>C	NP_001354777.1:n.-19+954T>C
NM_001367850.1:c.-19+954T>C	NP_001354779.1:n.-19+954T>C
NM_001367851.1:c.-134+954T>C	NP_001354780.1:n.-134+954T>C
NM_006757.4:c.-19+954T>C MANE Select	NP_006748.1:n.-19+954T>C
NM_001042780.3:c.-19+954T>C	NP_001036245.1:n.-19+954T>C
NM_001042781.3:c.-19+954T>C	NP_001036246.1:n.-19+954T>C
NM_001042782.3:c.-19+954T>C	NP_001036247.1:n.-19+954T>C
NM_001297646.2:c.-276-646T>C	NP_001284575.1:n.-276-646T>C
NM_001363561.2:c.-19+954T>C	NP_001350490.1:n.-19+954T>C