Canonical Allele Identifier: CA407441920

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55156295-C-G
• MyVariant Identifiers: chr19:g.55667663C>G (hg19) ; chr19:g.55156295C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156295C>G , CM000681.2:g.55156295C>G	GRCh38
NC_000019.9:g.55667663C>G , CM000681.1:g.55667663C>G	GRCh37
NC_000019.8:g.60359475C>G	NCBI36
NG_007866.2:g.6438G>C , LRG_432:g.6438G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.188G>C MANE Select	ENSP00000341838.5:p.Arg63Pro
ENST00000665070.1:c.188G>C	ENSP00000499482.1:p.Arg63Pro
ENST00000344887.9:c.188G>C	ENSP00000341838.5:p.Arg63Pro
ENST00000585806.5:n.187G>C
ENST00000586669.5:n.196G>C
ENST00000586858.1:c.151G>C	ENSP00000465258.1:p.Glu51Gln
ENST00000587176.5:n.372G>C
ENST00000587871.1:c.807G>C
ENST00000588882.1:c.113G>C	ENSP00000466729.1:p.Arg38Pro
ENST00000590463.1:n.360G>C
NM_000363.4:c.188G>C , LRG_432t1:c.188G>C	NP_000354.4:p.Arg63Pro
NM_000363.5:c.188G>C MANE Select	NP_000354.4:p.Arg63Pro