Canonical Allele Identifier: CA508989436

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55665506C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154138C>A , CM000681.2:g.55154138C>A	GRCh38
NC_000019.9:g.55665506C>A , CM000681.1:g.55665506C>A	GRCh37
NC_000019.8:g.60357318C>A	NCBI36
NG_007866.2:g.8595G>T , LRG_432:g.8595G>T
NG_011829.2:g.101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.441G>T MANE Select	ENSP00000341838.5:p.Val147=
ENST00000665070.1:c.474G>T	ENSP00000499482.1:p.Val158=
ENST00000344887.9:c.441G>T	ENSP00000341838.5:p.Val147=
ENST00000585806.5:n.440G>T
ENST00000586669.5:n.449G>T
ENST00000588882.1:c.366G>T	ENSP00000466729.1:p.Val122=
ENST00000589864.1:n.269G>T
NM_000363.4:c.441G>T , LRG_432t1:c.441G>T	NP_000354.4:p.Val147=
NM_000363.5:c.441G>T MANE Select	NP_000354.4:p.Val147=