Canonical Allele Identifier: CA508989382

Gene: TNNI3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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