Canonical Allele Identifier: CA340786854

Gene: TNNI3K FPGT-TNNI3K

Linked Data

• MyVariant Identifiers: chr1:g.74867523G>C (hg19) ; chr1:g.74401839G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.74401839G>C , CM000663.2:g.74401839G>C	GRCh38
NC_000001.10:g.74867523G>C , CM000663.1:g.74867523G>C	GRCh37
NC_000001.9:g.74640111G>C	NCBI36
NG_032939.2:g.208587G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326637.8:c.1772+31447G>C (TNNI3K) MANE Select	ENSP00000322251.3:n.1772+31447G>C
ENST00000557284.7:c.2075+31447G>C (FPGT-TNNI3K)	ENSP00000450895.3:n.2075+31447G>C
ENST00000648585.1:c.*1678+31447G>C (FPGT-TNNI3K)	ENSP00000497631.1:n.*1678+31447G>C
ENST00000326637.7:c.1772+31447G>C (TNNI3K)	ENSP00000322251.3:n.1772+31447G>C
ENST00000370899.7:c.2075+31447G>C (FPGT-TNNI3K)	ENSP00000359936.3:n.2075+31447G>C
ENST00000525480.2:c.332-16329G>C (TNNI3K)
ENST00000534020.5:c.345G>C (TNNI3K)	ENSP00000434975.1:p.Arg115Ser
ENST00000557284.6:c.2114+31447G>C (FPGT-TNNI3K)	ENSP00000450895.2:n.2114+31447G>C
NM_001112808.2:c.2114+31447G>C (FPGT-TNNI3K)	NP_001106279.2:n.2114+31447G>C
NM_001199327.1:c.2114+31447G>C (FPGT-TNNI3K)	NP_001186256.2:n.2114+31447G>C
NM_015978.2:c.1772+31447G>C (TNNI3K)	NP_057062.1:n.1772+31447G>C
NM_015978.3:c.1772+31447G>C (TNNI3K) MANE Select	NP_057062.1:n.1772+31447G>C
NM_001112808.3:c.2075+31447G>C (FPGT-TNNI3K)	NP_001106279.3:n.2075+31447G>C
NM_001199327.2:c.2075+31447G>C (FPGT-TNNI3K)	NP_001186256.3:n.2075+31447G>C