Canonical Allele Identifier: CA349661782

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501444A>T (hg19) ; chr2:g.178636717A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636717A>T , CM000664.2:g.178636717A>T	GRCh38
NC_000002.11:g.179501444A>T , CM000664.1:g.179501444A>T	GRCh37
NC_000002.10:g.179209689A>T	NCBI36
NG_011618.3:g.199086T>A , LRG_391:g.199086T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33306T>A	ENSP00000343764.6:p.Asp11102Glu
ENST00000342175.11:c.14391T>A	ENSP00000340554.6:p.Asp4797Glu
ENST00000359218.10:c.14190T>A	ENSP00000352154.5:p.Asp4730Glu
ENST00000342175.10:c.14391T>A	ENSP00000340554.6:p.Asp4797Glu
ENST00000342992.10:c.33306T>A	ENSP00000343764.6:p.Asp11102Glu
ENST00000359218.9:c.14190T>A	ENSP00000352154.5:p.Asp4730Glu
ENST00000460472.6:c.13815T>A	ENSP00000434586.1:p.Asp4605Glu
ENST00000589042.5:c.41010T>A MANE Select	ENSP00000467141.1:p.Asp13670Glu
ENST00000591111.5:c.36087T>A	ENSP00000465570.1:p.Asp12029Glu
ENST00000615779.4:c.36087T>A	ENSP00000483597.1:p.Asp12029Glu
NM_001256850.1:c.36087T>A	NP_001243779.1:p.Asp12029Glu
NM_001267550.2:c.41010T>A MANE Select	NP_001254479.2:p.Asp13670Glu
NM_003319.4:c.13815T>A	NP_003310.4:p.Asp4605Glu
NM_133378.4:c.33306T>A	NP_596869.4:p.Asp11102Glu
NM_133432.3:c.14190T>A	NP_597676.3:p.Asp4730Glu
NM_133437.4:c.14391T>A	NP_597681.4:p.Asp4797Glu
XM_011511729.1:c.40107T>A	XP_011510031.1:p.Asp13369Glu
XM_011511730.1:c.14001T>A	XP_011510032.1:p.Asp4667Glu
XM_011511731.1:c.13860T>A	XP_011510033.1:p.Asp4620Glu
XM_017004819.1:c.39903T>A	XP_016860308.1:p.Asp13301Glu
XM_017004820.1:c.35301T>A	XP_016860309.1:p.Asp11767Glu
XM_017004821.1:c.35298T>A	XP_016860310.1:p.Asp11766Glu
XM_017004822.1:c.32340T>A	XP_016860311.1:p.Asp10780Glu
XM_017004823.1:c.13956T>A	XP_016860312.1:p.Asp4652Glu
XM_024453094.1:c.35451T>A	XP_024308862.1:p.Asp11817Glu
XM_024453095.1:c.35448T>A	XP_024308863.1:p.Asp11816Glu
XM_024453096.1:c.34881T>A	XP_024308864.1:p.Asp11627Glu
XM_024453097.1:c.32223T>A	XP_024308865.1:p.Asp10741Glu
XM_024453098.1:c.32142T>A	XP_024308866.1:p.Asp10714Glu
XM_024453099.1:c.13905T>A	XP_024308867.1:p.Asp4635Glu
XM_024453100.1:c.3759T>A	XP_024308868.1:p.Asp1253Glu