Canonical Allele Identifier: CA2343264150

Gene: TNNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55137176C= , CM000681.2:g.55137176C=	GRCh38
NC_000019.9:g.55648544C= , CM000681.1:g.55648544C=	GRCh37
NC_000019.8:g.60340356C=	NCBI36
NG_011829.2:g.17063G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003283.6:c.538G= MANE Select	NP_003274.3:p.Glu180=
ENST00000588981.6:c.538G= MANE Select	ENSP00000467176.1:p.Glu180=
NM_001126132.2:c.538G=	NP_001119604.1:p.Glu180=
NM_001126132.3:c.538G=	NP_001119604.1:p.Glu180=
NM_001126133.2:c.505G=	NP_001119605.1:p.Glu169=
NM_001126133.3:c.505G=	NP_001119605.1:p.Glu169=
NM_001291774.1:c.505G=	NP_001278703.1:p.Glu169=
NM_001291774.2:c.505G=	NP_001278703.1:p.Glu169=
NM_003283.5:c.538G=	NP_003274.3:p.Glu180=
ENST00000291901.12:c.538G=	ENSP00000291901.8:p.Glu180=
ENST00000356783.9:c.505G=	ENSP00000349233.4:p.Glu169=
ENST00000536926.5:c.328G=	ENSP00000439640.2:p.Glu110=
ENST00000585321.6:c.328G=	ENSP00000467980.2:p.Glu110=
ENST00000586649.2:c.2G=
ENST00000587089.6:c.590G=
ENST00000587465.6:c.328G=	ENSP00000464843.2:p.Glu110=
ENST00000587758.5:c.505G=	ENSP00000467789.1:p.Glu169=
ENST00000588426.5:c.229G=	ENSP00000465991.1:p.Glu77=
ENST00000588981.5:c.538G=	ENSP00000467176.1:p.Glu180=
ENST00000589745.5:c.191G=
ENST00000593046.5:c.538G=	ENSP00000470777.1:p.Glu180=
ENST00000593194.5:c.381G=
XM_006723343.2:c.574G=	XP_006723406.1:p.Glu192=
XM_011527243.1:c.562G=	XP_011525545.1:p.Glu188=
XM_011527244.1:c.541G=	XP_011525546.1:p.Glu181=
XM_011527245.1:c.538G=	XP_011525547.1:p.Glu180=
XM_011527246.1:c.526G=	XP_011525548.1:p.Glu176=
XM_011527246.3:c.526G=	XP_011525548.1:p.Glu176=
XM_017027186.1:c.538G=	XP_016882675.1:p.Glu180=
XM_017027187.1:c.526G=	XP_016882676.1:p.Glu176=