Canonical Allele Identifier: CA508989337

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663235T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151867T>A , CM000681.2:g.55151867T>A	GRCh38
NC_000019.9:g.55663235T>A , CM000681.1:g.55663235T>A	GRCh37
NC_000019.8:g.60355047T>A	NCBI36
NG_007866.2:g.10866A>T , LRG_432:g.10866A>T
NG_011829.2:g.2372A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.600A>T MANE Select	ENSP00000341838.5:p.Gly200=
ENST00000665070.1:c.633A>T	ENSP00000499482.1:p.Gly211=
ENST00000344887.9:c.600A>T	ENSP00000341838.5:p.Gly200=
ENST00000585806.5:n.599A>T
ENST00000588882.1:c.525A>T	ENSP00000466729.1:p.Gly175=
ENST00000589864.1:n.428A>T
NM_000363.4:c.600A>T , LRG_432t1:c.600A>T	NP_000354.4:p.Gly200=
NM_000363.5:c.600A>T MANE Select	NP_000354.4:p.Gly200=