Canonical Allele Identifier: CA407440298

Gene: TNNI3

Linked Data

• gnomAD v4: 19-55154067-G-T
• MyVariant Identifiers: chr19:g.55665435G>T (hg19) ; chr19:g.55154067G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154067G>T , CM000681.2:g.55154067G>T	GRCh38
NC_000019.9:g.55665435G>T , CM000681.1:g.55665435G>T	GRCh37
NC_000019.8:g.60357247G>T	NCBI36
NG_007866.2:g.8666C>A , LRG_432:g.8666C>A
NG_011829.2:g.172C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.512C>A MANE Select	ENSP00000341838.5:p.Ala171Asp
ENST00000665070.1:c.545C>A	ENSP00000499482.1:p.Ala182Asp
ENST00000344887.9:c.512C>A	ENSP00000341838.5:p.Ala171Asp
ENST00000585806.5:n.511C>A
ENST00000588882.1:c.437C>A	ENSP00000466729.1:p.Ala146Asp
ENST00000589864.1:n.340C>A
NM_000363.4:c.512C>A , LRG_432t1:c.512C>A	NP_000354.4:p.Ala171Asp
NM_000363.5:c.512C>A MANE Select	NP_000354.4:p.Ala171Asp