Canonical Allele Identifier: CA407440472

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665496C>A (hg19) ; chr19:g.55154128C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154128C>A , CM000681.2:g.55154128C>A	GRCh38
NC_000019.9:g.55665496C>A , CM000681.1:g.55665496C>A	GRCh37
NC_000019.8:g.60357308C>A	NCBI36
NG_007866.2:g.8605G>T , LRG_432:g.8605G>T
NG_011829.2:g.111G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.451G>T MANE Select	ENSP00000341838.5:p.Ala151Ser
ENST00000665070.1:c.484G>T	ENSP00000499482.1:p.Ala162Ser
ENST00000344887.9:c.451G>T	ENSP00000341838.5:p.Ala151Ser
ENST00000585806.5:n.450G>T
ENST00000586669.5:n.459G>T
ENST00000588882.1:c.376G>T	ENSP00000466729.1:p.Ala126Ser
ENST00000589864.1:n.279G>T
NM_000363.4:c.451G>T , LRG_432t1:c.451G>T	NP_000354.4:p.Ala151Ser
NM_000363.5:c.451G>T MANE Select	NP_000354.4:p.Ala151Ser