Canonical Allele Identifier: CA9667432

Gene: TNNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55140867_55140872del , CM000681.2:g.55140867_55140872del	GRCh38
NC_000019.9:g.55652235_55652240del , CM000681.1:g.55652235_55652240del	GRCh37
NC_000019.8:g.60344047_60344052del	NCBI36
NG_011829.2:g.13370_13375del

Transcript Alleles

HGVS	Amino-acid Change
NM_003283.6:c.387+14_387+19del MANE Select	NP_003274.3:n.387+14_387+19del
ENST00000588981.6:c.387+14_387+19del MANE Select	ENSP00000467176.1:n.387+14_387+19del
NM_001126132.2:c.387+14_387+19del	NP_001119604.1:n.387+14_387+19del
NM_001126132.3:c.387+14_387+19del	NP_001119604.1:n.387+14_387+19del
NM_001126133.2:c.354+14_354+19del	NP_001119605.1:n.354+14_354+19del
NM_001126133.3:c.354+14_354+19del	NP_001119605.1:n.354+14_354+19del
NM_001291774.1:c.354+14_354+19del	NP_001278703.1:n.354+14_354+19del
NM_001291774.2:c.354+14_354+19del	NP_001278703.1:n.354+14_354+19del
NM_003283.5:c.387+14_387+19del	NP_003274.3:n.387+14_387+19del
ENST00000291901.12:c.387+14_387+19del	ENSP00000291901.8:n.387+14_387+19del
ENST00000356783.9:c.354+14_354+19del	ENSP00000349233.4:n.354+14_354+19del
ENST00000536926.5:c.177+14_177+19del	ENSP00000439640.2:n.177+14_177+19del
ENST00000585321.6:c.177+14_177+19del	ENSP00000467980.2:n.177+14_177+19del
ENST00000587089.6:c.439+14_439+19del
ENST00000587465.6:c.177+14_177+19del	ENSP00000464843.2:n.177+14_177+19del
ENST00000587758.5:c.354+14_354+19del	ENSP00000467789.1:n.354+14_354+19del
ENST00000588147.5:c.375+14_375+19del	ENSP00000467299.1:n.375+14_375+19del
ENST00000588426.5:c.78+14_78+19del	ENSP00000465991.1:n.78+14_78+19del
ENST00000588981.5:c.387+14_387+19del	ENSP00000467176.1:n.387+14_387+19del
ENST00000589226.5:c.354+14_354+19del	ENSP00000470854.1:n.354+14_354+19del
ENST00000589745.5:c.40+14_40+19del
ENST00000592920.5:n.465+14_465+19del
ENST00000593046.5:c.387+14_387+19del	ENSP00000470777.1:n.387+14_387+19del
ENST00000593194.5:c.230+14_230+19del
XM_006723343.2:c.423+14_423+19del	XP_006723406.1:n.423+14_423+19del
XM_011527243.1:c.411+14_411+19del	XP_011525545.1:n.411+14_411+19del
XM_011527244.1:c.390+14_390+19del	XP_011525546.1:n.390+14_390+19del
XM_011527245.1:c.387+14_387+19del	XP_011525547.1:n.387+14_387+19del
XM_011527246.1:c.375+14_375+19del	XP_011525548.1:n.375+14_375+19del
XM_011527246.3:c.375+14_375+19del	XP_011525548.1:n.375+14_375+19del
XM_017027186.1:c.387+14_387+19del	XP_016882675.1:n.387+14_387+19del
XM_017027187.1:c.375+14_375+19del	XP_016882676.1:n.375+14_375+19del