Canonical Allele Identifier: CA090659

Gene: TNNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359011C>T , CM000663.2:g.201359011C>T	GRCh38
NC_000001.10:g.201328139C>T , CM000663.1:g.201328139C>T	GRCh37
NC_000001.9:g.199594762C>T	NCBI36
NG_007556.1:g.23667G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*199G>A	ENSP00000402238.3:n.*199G>A
ENST00000660295.1:c.*199G>A	ENSP00000499418.1:n.*199G>A
ENST00000662159.1:c.*455G>A	ENSP00000499796.1:n.*455G>A
ENST00000236918.11:c.1096G>A	ENSP00000236918.8:n.1096G>A
ENST00000360372.8:c.967G>A	ENSP00000353535.5:n.967G>A
ENST00000367317.8:c.1048G>A	ENSP00000356286.5:n.1048G>A
ENST00000367318.9:c.*199G>A	ENSP00000356287.5:n.*199G>A
ENST00000367322.5:c.*199G>A	ENSP00000356291.1:n.*199G>A
ENST00000458432.6:c.*199G>A	ENSP00000387874.3:n.*199G>A
ENST00000460780.5:n.2215G>A
ENST00000476888.5:n.513G>A
ENST00000491504.5:n.2305G>A
NM_000364.3:c.*199G>A	NP_000355.2:n.*199G>A
NM_001001430.2:c.*199G>A	NP_001001430.1:n.*199G>A
NM_001001431.2:c.*199G>A	NP_001001431.1:n.*199G>A
NM_001001432.2:c.*199G>A	NP_001001432.1:n.*199G>A
NM_001276345.1:c.*199G>A	NP_001263274.1:n.*199G>A
NM_001276346.1:c.*199G>A	NP_001263275.1:n.*199G>A
NM_001276347.1:c.*199G>A	NP_001263276.1:n.*199G>A