Canonical Allele Identifier: CA997250983

Gene: TNNT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55138090G>A , CM000681.2:g.55138090G>A	GRCh38
NC_000019.9:g.55649458G>A , CM000681.1:g.55649458G>A	GRCh37
NC_000019.8:g.60341270G>A	NCBI36
NG_011829.2:g.16149C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003283.6:c.388-16C>T MANE Select	NP_003274.3:n.388-16C>T
ENST00000588981.6:c.388-16C>T MANE Select	ENSP00000467176.1:n.388-16C>T
NM_001126132.2:c.388-16C>T	NP_001119604.1:n.388-16C>T
NM_001126132.3:c.388-16C>T	NP_001119604.1:n.388-16C>T
NM_001126133.2:c.355-16C>T	NP_001119605.1:n.355-16C>T
NM_001126133.3:c.355-16C>T	NP_001119605.1:n.355-16C>T
NM_001291774.1:c.355-16C>T	NP_001278703.1:n.355-16C>T
NM_001291774.2:c.355-16C>T	NP_001278703.1:n.355-16C>T
NM_003283.5:c.388-16C>T	NP_003274.3:n.388-16C>T
ENST00000291901.12:c.388-16C>T	ENSP00000291901.8:n.388-16C>T
ENST00000356783.9:c.355-16C>T	ENSP00000349233.4:n.355-16C>T
ENST00000536926.5:c.178-16C>T	ENSP00000439640.2:n.178-16C>T
ENST00000585321.6:c.178-16C>T	ENSP00000467980.2:n.178-16C>T
ENST00000587089.6:c.440-16C>T
ENST00000587465.6:c.178-16C>T	ENSP00000464843.2:n.178-16C>T
ENST00000587758.5:c.355-16C>T	ENSP00000467789.1:n.355-16C>T
ENST00000588147.5:c.376-16C>T	ENSP00000467299.1:n.376-16C>T
ENST00000588426.5:c.79-16C>T	ENSP00000465991.1:n.79-16C>T
ENST00000588981.5:c.388-16C>T	ENSP00000467176.1:n.388-16C>T
ENST00000589226.5:c.355-16C>T	ENSP00000470854.1:n.355-16C>T
ENST00000589745.5:c.41-16C>T
ENST00000592920.5:n.514-16C>T
ENST00000593046.5:c.388-16C>T	ENSP00000470777.1:n.388-16C>T
ENST00000593194.5:c.231-16C>T
XM_006723343.2:c.424-16C>T	XP_006723406.1:n.424-16C>T
XM_011527243.1:c.412-16C>T	XP_011525545.1:n.412-16C>T
XM_011527244.1:c.391-16C>T	XP_011525546.1:n.391-16C>T
XM_011527245.1:c.388-16C>T	XP_011525547.1:n.388-16C>T
XM_011527246.1:c.376-16C>T	XP_011525548.1:n.376-16C>T
XM_011527246.3:c.376-16C>T	XP_011525548.1:n.376-16C>T
XM_017027186.1:c.388-16C>T	XP_016882675.1:n.388-16C>T
XM_017027187.1:c.376-16C>T	XP_016882676.1:n.376-16C>T