Canonical Allele Identifier: CA508989383

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665437C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154069C>G , CM000681.2:g.55154069C>G	GRCh38
NC_000019.9:g.55665437C>G , CM000681.1:g.55665437C>G	GRCh37
NC_000019.8:g.60357249C>G	NCBI36
NG_007866.2:g.8664G>C , LRG_432:g.8664G>C
NG_011829.2:g.170G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.510G>C MANE Select	ENSP00000341838.5:p.Arg170=
ENST00000665070.1:c.543G>C	ENSP00000499482.1:p.Arg181=
ENST00000344887.9:c.510G>C	ENSP00000341838.5:p.Arg170=
ENST00000585806.5:n.509G>C
ENST00000588882.1:c.435G>C	ENSP00000466729.1:p.Arg145=
ENST00000589864.1:n.338G>C
NM_000363.4:c.510G>C , LRG_432t1:c.510G>C	NP_000354.4:p.Arg170=
NM_000363.5:c.510G>C MANE Select	NP_000354.4:p.Arg170=