Canonical Allele Identifier: CA2343272787

Gene: TNNI3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55152168_55152172delinsACTTT , CM000681.2:g.55152168_55152172delinsACTTT	GRCh38
NC_000019.9:g.55663536_55663540delinsACTTT , CM000681.1:g.55663536_55663540delinsACTTT	GRCh37
NC_000019.8:g.60355348_60355352delinsACTTT	NCBI36
NG_007866.2:g.10561_10565delinsAAAGT , LRG_432:g.10561_10565delinsAAAGT
NG_011829.2:g.2067_2071delinsAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.550-255_550-251delinsAAAGT MANE Select	ENSP00000341838.5:n.550-255_550-251delinsAAAGT
ENST00000665070.1:c.583-255_583-251delinsAAAGT	ENSP00000499482.1:n.583-255_583-251delinsAAAGT
ENST00000344887.9:c.550-255_550-251delinsAAAGT	ENSP00000341838.5:n.550-255_550-251delinsAAAGT
ENST00000585806.5:n.549-255_549-251delinsAAAGT
ENST00000588882.1:c.475-255_475-251delinsAAAGT	ENSP00000466729.1:n.475-255_475-251delinsAAAGT
ENST00000589864.1:n.378-255_378-251delinsAAAGT
NM_000363.4:c.550-255_550-251delinsAAAGT , LRG_432t1:c.550-255_550-251delinsAAAGT	NP_000354.4:n.550-255_550-251delinsAAAGT
NM_000363.5:c.550-255_550-251delinsAAAGT MANE Select	NP_000354.4:n.550-255_550-251delinsAAAGT