Canonical Allele Identifier: CA2580097802

Gene: TNNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55141848G>T , CM000681.2:g.55141848G>T	GRCh38
NC_000019.9:g.55653216G>T , CM000681.1:g.55653216G>T	GRCh37
NC_000019.8:g.60345028G>T	NCBI36
NG_011829.2:g.12391C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003283.6:c.192+9C>A MANE Select	NP_003274.3:n.192+9C>A
ENST00000588981.6:c.192+9C>A MANE Select	ENSP00000467176.1:n.192+9C>A
NM_001126132.2:c.192+9C>A	NP_001119604.1:n.192+9C>A
NM_001126132.3:c.192+9C>A	NP_001119604.1:n.192+9C>A
NM_001126133.2:c.159+9C>A	NP_001119605.1:n.159+9C>A
NM_001126133.3:c.159+9C>A	NP_001119605.1:n.159+9C>A
NM_001291774.1:c.159+9C>A	NP_001278703.1:n.159+9C>A
NM_001291774.2:c.159+9C>A	NP_001278703.1:n.159+9C>A
NM_003283.5:c.192+9C>A	NP_003274.3:n.192+9C>A
ENST00000291901.12:c.192+9C>A	ENSP00000291901.8:n.192+9C>A
ENST00000356783.9:c.159+9C>A	ENSP00000349233.4:n.159+9C>A
ENST00000536926.5:c.-19+9C>A	ENSP00000439640.2:n.-19+9C>A
ENST00000585321.6:c.-19+9C>A	ENSP00000467980.2:n.-19+9C>A
ENST00000587089.6:c.244+9C>A
ENST00000587465.6:c.-19+9C>A	ENSP00000464843.2:n.-19+9C>A
ENST00000587758.5:c.159+9C>A	ENSP00000467789.1:n.159+9C>A
ENST00000588147.5:c.180+9C>A	ENSP00000467299.1:n.180+9C>A
ENST00000588426.5:c.49-936C>A	ENSP00000465991.1:n.49-936C>A
ENST00000588981.5:c.192+9C>A	ENSP00000467176.1:n.192+9C>A
ENST00000589226.5:c.159+9C>A	ENSP00000470854.1:n.159+9C>A
ENST00000592920.5:n.270+9C>A
ENST00000593046.5:c.192+9C>A	ENSP00000470777.1:n.192+9C>A
ENST00000593194.5:c.35+9C>A
XM_006723343.2:c.228+9C>A	XP_006723406.1:n.228+9C>A
XM_011527243.1:c.216+9C>A	XP_011525545.1:n.216+9C>A
XM_011527244.1:c.195+9C>A	XP_011525546.1:n.195+9C>A
XM_011527245.1:c.192+9C>A	XP_011525547.1:n.192+9C>A
XM_011527246.1:c.180+9C>A	XP_011525548.1:n.180+9C>A
XM_011527246.3:c.180+9C>A	XP_011525548.1:n.180+9C>A
XM_017027186.1:c.192+9C>A	XP_016882675.1:n.192+9C>A
XM_017027187.1:c.180+9C>A	XP_016882676.1:n.180+9C>A