Canonical Allele Identifier: CA9667633

Gene: TNNT1

Linked Data

• ClinVar Variation Id: 259031
• ClinVar RCV Id: RCV000249732 ; RCV000553573 ; RCV001582852
• dbSNP Id: rs375682055
• ExAC: 19:55658081 G / C
• gnomAD v2: 19-55658081-G-C
• gnomAD v3: 19-55146713-G-C
• gnomAD v4: 19-55146713-G-C
• MyVariant Identifiers: chr19:g.55658081G>C (hg19) ; chr19:g.55146713G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55146713G>C , CM000681.2:g.55146713G>C	GRCh38
NC_000019.9:g.55658081G>C , CM000681.1:g.55658081G>C	GRCh37
NC_000019.8:g.60349893G>C	NCBI36
NG_011829.2:g.7526C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588981.6:c.47-6C>G MANE Select	ENSP00000467176.1:n.47-6C>G
ENST00000291901.12:c.47-6C>G	ENSP00000291901.8:n.47-6C>G
ENST00000356783.9:c.47-6C>G	ENSP00000349233.4:n.47-6C>G
ENST00000536926.5:c.-131-6C>G	ENSP00000439640.2:n.-131-6C>G
ENST00000585321.6:c.-137C>G	ENSP00000467980.2:n.-137C>G
ENST00000586282.1:n.104-8C>G
ENST00000587465.6:c.-170C>G	ENSP00000464843.2:n.-170C>G
ENST00000587758.5:c.47-6C>G	ENSP00000467789.1:n.47-6C>G
ENST00000588147.5:c.47-6C>G	ENSP00000467299.1:n.47-6C>G
ENST00000588426.5:c.22-6C>G	ENSP00000465991.1:n.22-6C>G
ENST00000588981.5:c.47-6C>G	ENSP00000467176.1:n.47-6C>G
ENST00000589226.5:c.47-6C>G	ENSP00000470854.1:n.47-6C>G
ENST00000592920.5:n.125-6C>G
ENST00000593046.5:c.47-6C>G	ENSP00000470777.1:n.47-6C>G
NM_001126132.2:c.47-6C>G	NP_001119604.1:n.47-6C>G
NM_001126133.2:c.47-6C>G	NP_001119605.1:n.47-6C>G
NM_001291774.1:c.47-6C>G	NP_001278703.1:n.47-6C>G
NM_003283.5:c.47-6C>G	NP_003274.3:n.47-6C>G
XM_006723343.2:c.77C>G	XP_006723406.1:p.Ser26Cys
XM_011527243.1:c.77C>G	XP_011525545.1:p.Ser26Cys
XM_011527244.1:c.77C>G	XP_011525546.1:p.Ser26Cys
XM_011527245.1:c.47-6C>G	XP_011525547.1:n.47-6C>G
XM_011527246.1:c.47-6C>G	XP_011525548.1:n.47-6C>G
XM_011527246.3:c.47-6C>G	XP_011525548.1:n.47-6C>G
XM_017027186.1:c.47-6C>G	XP_016882675.1:n.47-6C>G
XM_017027187.1:c.47-6C>G	XP_016882676.1:n.47-6C>G
NM_003283.6:c.47-6C>G MANE Select	NP_003274.3:n.47-6C>G
NM_001126132.3:c.47-6C>G	NP_001119604.1:n.47-6C>G
NM_001126133.3:c.47-6C>G	NP_001119605.1:n.47-6C>G
NM_001291774.2:c.47-6C>G	NP_001278703.1:n.47-6C>G