Canonical Allele Identifier: CA1003242629
Gene: TNNI3K HGNC NCBI
FPGT-TNNI3K HGNC NCBI

Linked Data

dbSNP Id: rs1664400836
gnomAD v3: 1-74402210-G-T
gnomAD v4: 1-74402210-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.74402210G>T , CM000663.2:g.74402210G>T GRCh38
NC_000001.10:g.74867894G>T , CM000663.1:g.74867894G>T GRCh37
NC_000001.9:g.74640482G>T NCBI36
NG_032939.2:g.208958G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326637.8:c.1772+31818G>T (TNNI3K) MANE Select ENSP00000322251.3:n.1772+31818G>T
ENST00000557284.7:c.2075+31818G>T (FPGT-TNNI3K) ENSP00000450895.3:n.2075+31818G>T
ENST00000648585.1:c.*1678+31818G>T (FPGT-TNNI3K) ENSP00000497631.1:n.*1678+31818G>T
ENST00000326637.7:c.1772+31818G>T (TNNI3K) ENSP00000322251.3:n.1772+31818G>T
ENST00000370899.7:c.2075+31818G>T (FPGT-TNNI3K) ENSP00000359936.3:n.2075+31818G>T
ENST00000525480.2:c.332-15958G>T (TNNI3K)
ENST00000534020.5:c.463+253G>T (TNNI3K) ENSP00000434975.1:n.463+253G>T
ENST00000557284.6:c.2114+31818G>T (FPGT-TNNI3K) ENSP00000450895.2:n.2114+31818G>T
NM_001112808.2:c.2114+31818G>T (FPGT-TNNI3K) NP_001106279.2:n.2114+31818G>T
NM_001199327.1:c.2114+31818G>T (FPGT-TNNI3K) NP_001186256.2:n.2114+31818G>T
NM_015978.2:c.1772+31818G>T (TNNI3K) NP_057062.1:n.1772+31818G>T
NM_015978.3:c.1772+31818G>T (TNNI3K) MANE Select NP_057062.1:n.1772+31818G>T
NM_001112808.3:c.2075+31818G>T (FPGT-TNNI3K) NP_001106279.3:n.2075+31818G>T
NM_001199327.2:c.2075+31818G>T (FPGT-TNNI3K) NP_001186256.3:n.2075+31818G>T