Canonical Allele Identifier: CA1219709310

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359010C= , CM000663.2:g.201359010C=	GRCh38
NC_000001.10:g.201328138C= , CM000663.1:g.201328138C=	GRCh37
NC_000001.9:g.199594761C=	NCBI36
NG_007556.1:g.23668G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*200G=	ENSP00000402238.3:n.*200G=
ENST00000660295.1:c.*200G=	ENSP00000499418.1:n.*200G=
ENST00000662159.1:c.*456G=	ENSP00000499796.1:n.*456G=
ENST00000236918.11:c.1097G=	ENSP00000236918.8:n.1097G=
ENST00000360372.8:c.968G=	ENSP00000353535.5:n.968G=
ENST00000367317.8:c.1049G=	ENSP00000356286.5:n.1049G=
ENST00000367318.9:c.*200G=	ENSP00000356287.5:n.*200G=
ENST00000367322.5:c.*200G=	ENSP00000356291.1:n.*200G=
ENST00000458432.6:c.*200G=	ENSP00000387874.3:n.*200G=
ENST00000460780.5:n.2216G=
ENST00000476888.5:n.514G=
ENST00000491504.5:n.2306G=
NM_000364.3:c.*200G=	NP_000355.2:n.*200G=
NM_001001430.2:c.*200G=	NP_001001430.1:n.*200G=
NM_001001431.2:c.*200G=	NP_001001431.1:n.*200G=
NM_001001432.2:c.*200G=	NP_001001432.1:n.*200G=
NM_001276345.1:c.*200G=	NP_001263274.1:n.*200G=
NM_001276346.1:c.*200G=	NP_001263275.1:n.*200G=
NM_001276347.1:c.*200G=	NP_001263276.1:n.*200G=