Canonical Allele Identifier: CA1176204604
Gene: TNNI3K HGNC NCBI
FPGT-TNNI3K HGNC NCBI
LRRC53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.74527281A= , CM000663.2:g.74527281A= GRCh38
NC_000001.10:g.74992965A= , CM000663.1:g.74992965A= GRCh37
NC_000001.9:g.74765553A= NCBI36
NG_032939.2:g.334029A=

Transcript Alleles

HGVS Amino-acid change
ENST00000326637.8:c.2352-12953A= (TNNI3K) MANE Select ENSP00000322251.3:n.2352-12953A=
ENST00000557284.7:c.2655-12953A= (FPGT-TNNI3K) ENSP00000450895.3:n.2655-12953A=
ENST00000648585.1:c.*2258-12953A= (FPGT-TNNI3K) ENSP00000497631.1:n.*2258-12953A=
ENST00000326637.7:c.2352-12953A= (TNNI3K) ENSP00000322251.3:n.2352-12953A=
ENST00000557284.6:c.2694-12953A= (FPGT-TNNI3K) ENSP00000450895.2:n.2694-12953A=
NM_001112808.2:c.2694-12953A= (FPGT-TNNI3K) NP_001106279.2:n.2694-12953A=
NM_015978.2:c.2352-12953A= (TNNI3K) NP_057062.1:n.2352-12953A=
XM_011542511.1:c.49+9523T= (LRRC53) XP_011540813.1:n.49+9523T=
XM_011542512.3:c.49+9523T= (LRRC53) XP_011540814.2:n.49+9523T=
XM_017003081.1:c.49+9523T= (LRRC53) XP_016858570.1:n.49+9523T=
NM_015978.3:c.2352-12953A= (TNNI3K) MANE Select NP_057062.1:n.2352-12953A=
NM_001112808.3:c.2655-12953A= (FPGT-TNNI3K) NP_001106279.3:n.2655-12953A=