Canonical Allele Identifier: CA633866042
Community Standard Title: NM_003283.6(TNNT1):c.193-14C>T
Gene: TNNT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55141316G>A , CM000681.2:g.55141316G>A GRCh38
NC_000019.9:g.55652684G>A , CM000681.1:g.55652684G>A GRCh37
NC_000019.8:g.60344496G>A NCBI36
NG_011829.2:g.12923C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003283.6:c.193-14C>T MANE Select NP_003274.3:n.193-14C>T
ENST00000588981.6:c.193-14C>T MANE Select ENSP00000467176.1:n.193-14C>T
NM_001126132.2:c.193-14C>T NP_001119604.1:n.193-14C>T
NM_001126132.3:c.193-14C>T NP_001119604.1:n.193-14C>T
NM_001126133.2:c.160-14C>T NP_001119605.1:n.160-14C>T
NM_001126133.3:c.160-14C>T NP_001119605.1:n.160-14C>T
NM_001291774.1:c.160-14C>T NP_001278703.1:n.160-14C>T
NM_001291774.2:c.160-14C>T NP_001278703.1:n.160-14C>T
NM_003283.5:c.193-14C>T NP_003274.3:n.193-14C>T
ENST00000291901.12:c.193-14C>T ENSP00000291901.8:n.193-14C>T
ENST00000356783.9:c.160-14C>T ENSP00000349233.4:n.160-14C>T
ENST00000536926.5:c.-18-14C>T ENSP00000439640.2:n.-18-14C>T
ENST00000585321.6:c.-18-14C>T ENSP00000467980.2:n.-18-14C>T
ENST00000587089.6:c.245-14C>T
ENST00000587465.6:c.-18-14C>T ENSP00000464843.2:n.-18-14C>T
ENST00000587758.5:c.160-14C>T ENSP00000467789.1:n.160-14C>T
ENST00000588147.5:c.181-14C>T ENSP00000467299.1:n.181-14C>T
ENST00000588426.5:c.49-404C>T ENSP00000465991.1:n.49-404C>T
ENST00000588981.5:c.193-14C>T ENSP00000467176.1:n.193-14C>T
ENST00000589226.5:c.160-14C>T ENSP00000470854.1:n.160-14C>T
ENST00000592920.5:n.271-14C>T
ENST00000593046.5:c.193-14C>T ENSP00000470777.1:n.193-14C>T
ENST00000593194.5:c.36-14C>T
XM_006723343.2:c.229-14C>T XP_006723406.1:n.229-14C>T
XM_011527243.1:c.217-14C>T XP_011525545.1:n.217-14C>T
XM_011527244.1:c.196-14C>T XP_011525546.1:n.196-14C>T
XM_011527245.1:c.193-14C>T XP_011525547.1:n.193-14C>T
XM_011527246.1:c.181-14C>T XP_011525548.1:n.181-14C>T
XM_011527246.3:c.181-14C>T XP_011525548.1:n.181-14C>T
XM_017027186.1:c.193-14C>T XP_016882675.1:n.193-14C>T
XM_017027187.1:c.181-14C>T XP_016882676.1:n.181-14C>T