Canonical Allele Identifier: CA1310556889

Gene: TTN

Linked Data

• dbSNP Id: rs2059972557

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178632872G>A , CM000664.2:g.178632872G>A	GRCh38
NC_000002.11:g.179497599G>A , CM000664.1:g.179497599G>A	GRCh37
NC_000002.10:g.179205844G>A	NCBI36
NG_011618.3:g.202931C>T , LRG_391:g.202931C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.35509+46C>T	ENSP00000343764.6:n.35509+46C>T
ENST00000342175.11:c.16594+46C>T	ENSP00000340554.6:n.16594+46C>T
ENST00000359218.10:c.16393+46C>T	ENSP00000352154.5:n.16393+46C>T
ENST00000342175.10:c.16594+46C>T	ENSP00000340554.6:n.16594+46C>T
ENST00000342992.10:c.35509+46C>T	ENSP00000343764.6:n.35509+46C>T
ENST00000359218.9:c.16393+46C>T	ENSP00000352154.5:n.16393+46C>T
ENST00000460472.6:c.16018+46C>T	ENSP00000434586.1:n.16018+46C>T
ENST00000589042.5:c.43213+46C>T MANE Select	ENSP00000467141.1:n.43213+46C>T
ENST00000591111.5:c.38290+46C>T	ENSP00000465570.1:n.38290+46C>T
ENST00000615779.4:c.38290+46C>T	ENSP00000483597.1:n.38290+46C>T
NM_001256850.1:c.38290+46C>T	NP_001243779.1:n.38290+46C>T
NM_001267550.2:c.43213+46C>T MANE Select	NP_001254479.2:n.43213+46C>T
NM_003319.4:c.16018+46C>T	NP_003310.4:n.16018+46C>T
NM_133378.4:c.35509+46C>T	NP_596869.4:n.35509+46C>T
NM_133432.3:c.16393+46C>T	NP_597676.3:n.16393+46C>T
NM_133437.4:c.16594+46C>T	NP_597681.4:n.16594+46C>T
XM_011511729.1:c.42310+46C>T	XP_011510031.1:n.42310+46C>T
XM_011511730.1:c.16204+46C>T	XP_011510032.1:n.16204+46C>T
XM_011511731.1:c.16063+46C>T	XP_011510033.1:n.16063+46C>T
XM_017004819.1:c.42106+46C>T	XP_016860308.1:n.42106+46C>T
XM_017004820.1:c.37504+46C>T	XP_016860309.1:n.37504+46C>T
XM_017004821.1:c.37501+46C>T	XP_016860310.1:n.37501+46C>T
XM_017004822.1:c.34543+46C>T	XP_016860311.1:n.34543+46C>T
XM_017004823.1:c.16159+46C>T	XP_016860312.1:n.16159+46C>T
XM_024453094.1:c.37654+46C>T	XP_024308862.1:n.37654+46C>T
XM_024453095.1:c.37651+46C>T	XP_024308863.1:n.37651+46C>T
XM_024453096.1:c.37084+46C>T	XP_024308864.1:n.37084+46C>T
XM_024453097.1:c.34426+46C>T	XP_024308865.1:n.34426+46C>T
XM_024453098.1:c.34345+46C>T	XP_024308866.1:n.34345+46C>T
XM_024453099.1:c.16108+46C>T	XP_024308867.1:n.16108+46C>T
XM_024453100.1:c.5962+46C>T	XP_024308868.1:n.5962+46C>T