Canonical Allele Identifier: CA1219709311

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359012A= , CM000663.2:g.201359012A=	GRCh38
NC_000001.10:g.201328140A= , CM000663.1:g.201328140A=	GRCh37
NC_000001.9:g.199594763A=	NCBI36
NG_007556.1:g.23666T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*198T=	ENSP00000402238.3:n.*198T=
ENST00000660295.1:c.*198T=	ENSP00000499418.1:n.*198T=
ENST00000662159.1:c.*454T=	ENSP00000499796.1:n.*454T=
ENST00000236918.11:c.1095T=	ENSP00000236918.8:n.1095T=
ENST00000360372.8:c.966T=	ENSP00000353535.5:n.966T=
ENST00000367317.8:c.1047T=	ENSP00000356286.5:n.1047T=
ENST00000367318.9:c.*198T=	ENSP00000356287.5:n.*198T=
ENST00000367322.5:c.*198T=	ENSP00000356291.1:n.*198T=
ENST00000458432.6:c.*198T=	ENSP00000387874.3:n.*198T=
ENST00000460780.5:n.2214T=
ENST00000476888.5:n.512T=
ENST00000491504.5:n.2304T=
NM_000364.3:c.*198T=	NP_000355.2:n.*198T=
NM_001001430.2:c.*198T=	NP_001001430.1:n.*198T=
NM_001001431.2:c.*198T=	NP_001001431.1:n.*198T=
NM_001001432.2:c.*198T=	NP_001001432.1:n.*198T=
NM_001276345.1:c.*198T=	NP_001263274.1:n.*198T=
NM_001276346.1:c.*198T=	NP_001263275.1:n.*198T=
NM_001276347.1:c.*198T=	NP_001263276.1:n.*198T=