Canonical Allele Identifier: CA407442001

Gene: TNNI3

Linked Data

• MyVariant Identifiers: chr19:g.55667680T>G (hg19) ; chr19:g.55156312T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55156312T>G , CM000681.2:g.55156312T>G	GRCh38
NC_000019.9:g.55667680T>G , CM000681.1:g.55667680T>G	GRCh37
NC_000019.8:g.60359492T>G	NCBI36
NG_007866.2:g.6421A>C , LRG_432:g.6421A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344887.10:c.171A>C MANE Select	ENSP00000341838.5:p.Ala57=
ENST00000665070.1:c.171A>C	ENSP00000499482.1:p.Ala57=
ENST00000344887.9:c.171A>C	ENSP00000341838.5:p.Ala57=
ENST00000585806.5:n.170A>C
ENST00000586669.5:n.179A>C
ENST00000586858.1:c.134A>C	ENSP00000465258.1:p.Gln45Pro
ENST00000587176.5:n.355A>C
ENST00000587871.1:c.790A>C
ENST00000588882.1:c.96A>C	ENSP00000466729.1:p.Ala32=
ENST00000590463.1:n.343A>C
NM_000363.4:c.171A>C , LRG_432t1:c.171A>C	NP_000354.4:p.Ala57=
NM_000363.5:c.171A>C MANE Select	NP_000354.4:p.Ala57=