Canonical Allele Identifier: CA407439497

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55151866-T-C
• MyVariant Identifiers: chr19:g.55663234T>C (hg19) ; chr19:g.55151866T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151866T>C , CM000681.2:g.55151866T>C	GRCh38
NC_000019.9:g.55663234T>C , CM000681.1:g.55663234T>C	GRCh37
NC_000019.8:g.60355046T>C	NCBI36
NG_007866.2:g.10867A>G , LRG_432:g.10867A>G
NG_011829.2:g.2373A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.601A>G MANE Select	ENSP00000341838.5:p.Met201Val
ENST00000665070.1:c.634A>G	ENSP00000499482.1:p.Met212Val
ENST00000344887.9:c.601A>G	ENSP00000341838.5:p.Met201Val
ENST00000585806.5:n.600A>G
ENST00000588882.1:c.526A>G	ENSP00000466729.1:p.Met176Val
ENST00000589864.1:n.429A>G
NM_000363.4:c.601A>G , LRG_432t1:c.601A>G	NP_000354.4:p.Met201Val
NM_000363.5:c.601A>G MANE Select	NP_000354.4:p.Met201Val