Canonical Allele Identifier: CA761292979

Gene: TTN

Linked Data

• dbSNP Id: rs1164234165
• MyVariant Identifiers: chr2:g.179494881_179494884del (hg19) ; chr2:g.178630154_178630157del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630154_178630157del , CM000664.2:g.178630154_178630157del	GRCh38
NC_000002.11:g.179494881_179494884del , CM000664.1:g.179494881_179494884del	GRCh37
NC_000002.10:g.179203126_179203129del	NCBI36
NG_011618.3:g.205646_205649del , LRG_391:g.205646_205649del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36577+84_36577+87del	ENSP00000343764.6:n.36577+84_36577+87del
ENST00000342175.11:c.17662+84_17662+87del	ENSP00000340554.6:n.17662+84_17662+87del
ENST00000359218.10:c.17461+84_17461+87del	ENSP00000352154.5:n.17461+84_17461+87del
ENST00000342175.10:c.17662+84_17662+87del	ENSP00000340554.6:n.17662+84_17662+87del
ENST00000342992.10:c.36577+84_36577+87del	ENSP00000343764.6:n.36577+84_36577+87del
ENST00000359218.9:c.17461+84_17461+87del	ENSP00000352154.5:n.17461+84_17461+87del
ENST00000460472.6:c.17086+84_17086+87del	ENSP00000434586.1:n.17086+84_17086+87del
ENST00000589042.5:c.44281+84_44281+87del MANE Select	ENSP00000467141.1:n.44281+84_44281+87del
ENST00000591111.5:c.39358+84_39358+87del	ENSP00000465570.1:n.39358+84_39358+87del
ENST00000615779.4:c.39358+84_39358+87del	ENSP00000483597.1:n.39358+84_39358+87del
NM_001256850.1:c.39358+84_39358+87del	NP_001243779.1:n.39358+84_39358+87del
NM_001267550.2:c.44281+84_44281+87del MANE Select	NP_001254479.2:n.44281+84_44281+87del
NM_003319.4:c.17086+84_17086+87del	NP_003310.4:n.17086+84_17086+87del
NM_133378.4:c.36577+84_36577+87del	NP_596869.4:n.36577+84_36577+87del
NM_133432.3:c.17461+84_17461+87del	NP_597676.3:n.17461+84_17461+87del
NM_133437.4:c.17662+84_17662+87del	NP_597681.4:n.17662+84_17662+87del
XM_011511729.1:c.43378+84_43378+87del	XP_011510031.1:n.43378+84_43378+87del
XM_011511730.1:c.17272+84_17272+87del	XP_011510032.1:n.17272+84_17272+87del
XM_011511731.1:c.17131+84_17131+87del	XP_011510033.1:n.17131+84_17131+87del
XM_017004819.1:c.43174+84_43174+87del	XP_016860308.1:n.43174+84_43174+87del
XM_017004820.1:c.38572+84_38572+87del	XP_016860309.1:n.38572+84_38572+87del
XM_017004821.1:c.38569+84_38569+87del	XP_016860310.1:n.38569+84_38569+87del
XM_017004822.1:c.35611+84_35611+87del	XP_016860311.1:n.35611+84_35611+87del
XM_017004823.1:c.17227+84_17227+87del	XP_016860312.1:n.17227+84_17227+87del
XM_024453094.1:c.38722+84_38722+87del	XP_024308862.1:n.38722+84_38722+87del
XM_024453095.1:c.38719+84_38719+87del	XP_024308863.1:n.38719+84_38719+87del
XM_024453096.1:c.38152+84_38152+87del	XP_024308864.1:n.38152+84_38152+87del
XM_024453097.1:c.35494+84_35494+87del	XP_024308865.1:n.35494+84_35494+87del
XM_024453098.1:c.35413+84_35413+87del	XP_024308866.1:n.35413+84_35413+87del
XM_024453099.1:c.17176+84_17176+87del	XP_024308867.1:n.17176+84_17176+87del
XM_024453100.1:c.7030+84_7030+87del	XP_024308868.1:n.7030+84_7030+87del