Canonical Allele Identifier: CA2649785721

Gene: TNNT2

Linked Data

• gnomAD v4: 1-201359009-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359009G>T , CM000663.2:g.201359009G>T	GRCh38
NC_000001.10:g.201328137G>T , CM000663.1:g.201328137G>T	GRCh37
NC_000001.9:g.199594760G>T	NCBI36
NG_007556.1:g.23669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*201C>A	ENSP00000402238.3:n.*201C>A
ENST00000660295.1:c.*201C>A	ENSP00000499418.1:n.*201C>A
ENST00000662159.1:c.*457C>A	ENSP00000499796.1:n.*457C>A
ENST00000236918.11:c.1098C>A	ENSP00000236918.8:n.1098C>A
ENST00000360372.8:c.969C>A	ENSP00000353535.5:n.969C>A
ENST00000367317.8:c.1050C>A	ENSP00000356286.5:n.1050C>A
ENST00000367318.9:c.*201C>A	ENSP00000356287.5:n.*201C>A
ENST00000367322.5:c.*201C>A	ENSP00000356291.1:n.*201C>A
ENST00000458432.6:c.*201C>A	ENSP00000387874.3:n.*201C>A
ENST00000460780.5:n.2217C>A
ENST00000476888.5:n.515C>A
ENST00000491504.5:n.2307C>A
NM_000364.3:c.*201C>A	NP_000355.2:n.*201C>A
NM_001001430.2:c.*201C>A	NP_001001430.1:n.*201C>A
NM_001001431.2:c.*201C>A	NP_001001431.1:n.*201C>A
NM_001001432.2:c.*201C>A	NP_001001432.1:n.*201C>A
NM_001276345.1:c.*201C>A	NP_001263274.1:n.*201C>A
NM_001276346.1:c.*201C>A	NP_001263275.1:n.*201C>A
NM_001276347.1:c.*201C>A	NP_001263276.1:n.*201C>A