Canonical Allele Identifier: CA407439642

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55663266T>G (hg19) ; chr19:g.55151898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151898T>G , CM000681.2:g.55151898T>G	GRCh38
NC_000019.9:g.55663266T>G , CM000681.1:g.55663266T>G	GRCh37
NC_000019.8:g.60355078T>G	NCBI36
NG_007866.2:g.10835A>C , LRG_432:g.10835A>C
NG_011829.2:g.2341A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.569A>C MANE Select	ENSP00000341838.5:p.Asp190Ala
ENST00000665070.1:c.602A>C	ENSP00000499482.1:p.Asp201Ala
ENST00000344887.9:c.569A>C	ENSP00000341838.5:p.Asp190Ala
ENST00000585806.5:n.568A>C
ENST00000588882.1:c.494A>C	ENSP00000466729.1:p.Asp165Ala
ENST00000589864.1:n.397A>C
NM_000363.4:c.569A>C , LRG_432t1:c.569A>C	NP_000354.4:p.Asp190Ala
NM_000363.5:c.569A>C MANE Select	NP_000354.4:p.Asp190Ala