Canonical Allele Identifier: CA9667316

Gene: TNNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55134090C>T , CM000681.2:g.55134090C>T	GRCh38
NC_000019.9:g.55645458C>T , CM000681.1:g.55645458C>T	GRCh37
NC_000019.8:g.60337270C>T	NCBI36
NG_011829.2:g.20149G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003283.6:c.726G>A MANE Select	NP_003274.3:p.Ala242=
ENST00000588981.6:c.726G>A MANE Select	ENSP00000467176.1:p.Ala242=
NM_001126132.2:c.678G>A	NP_001119604.1:p.Ala226=
NM_001126132.3:c.678G>A	NP_001119604.1:p.Ala226=
NM_001126133.2:c.645G>A	NP_001119605.1:p.Ala215=
NM_001126133.3:c.645G>A	NP_001119605.1:p.Ala215=
NM_001291774.1:c.645G>A	NP_001278703.1:p.Ala215=
NM_001291774.2:c.645G>A	NP_001278703.1:p.Ala215=
NM_003283.5:c.726G>A	NP_003274.3:p.Ala242=
ENST00000291901.12:c.678G>A	ENSP00000291901.8:p.Ala226=
ENST00000356783.9:c.645G>A	ENSP00000349233.4:p.Ala215=
ENST00000536926.5:c.468G>A	ENSP00000439640.2:p.Ala156=
ENST00000585321.6:c.468G>A	ENSP00000467980.2:p.Ala156=
ENST00000586649.2:c.142G>A
ENST00000587089.6:c.730G>A
ENST00000587465.6:c.468G>A	ENSP00000464843.2:p.Ala156=
ENST00000587758.5:c.645G>A	ENSP00000467789.1:p.Ala215=
ENST00000588426.5:c.369G>A	ENSP00000465991.1:p.Ala123=
ENST00000588981.5:c.726G>A	ENSP00000467176.1:p.Ala242=
ENST00000589745.5:c.331G>A
ENST00000593194.5:c.521G>A
XM_006723343.2:c.714G>A	XP_006723406.1:p.Ala238=
XM_011527243.1:c.702G>A	XP_011525545.1:p.Ala234=
XM_011527244.1:c.681G>A	XP_011525546.1:p.Ala227=
XM_011527245.1:c.678G>A	XP_011525547.1:p.Ala226=
XM_011527246.1:c.666G>A	XP_011525548.1:p.Ala222=
XM_011527246.3:c.666G>A	XP_011525548.1:p.Ala222=
XM_017027186.1:c.678G>A	XP_016882675.1:p.Ala226=
XM_017027187.1:c.666G>A	XP_016882676.1:p.Ala222=