Canonical Allele Identifier: CA349661789

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501446C>A (hg19) ; chr2:g.178636719C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636719C>A , CM000664.2:g.178636719C>A	GRCh38
NC_000002.11:g.179501446C>A , CM000664.1:g.179501446C>A	GRCh37
NC_000002.10:g.179209691C>A	NCBI36
NG_011618.3:g.199084G>T , LRG_391:g.199084G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33304G>T	ENSP00000343764.6:p.Asp11102Tyr
ENST00000342175.11:c.14389G>T	ENSP00000340554.6:p.Asp4797Tyr
ENST00000359218.10:c.14188G>T	ENSP00000352154.5:p.Asp4730Tyr
ENST00000342175.10:c.14389G>T	ENSP00000340554.6:p.Asp4797Tyr
ENST00000342992.10:c.33304G>T	ENSP00000343764.6:p.Asp11102Tyr
ENST00000359218.9:c.14188G>T	ENSP00000352154.5:p.Asp4730Tyr
ENST00000460472.6:c.13813G>T	ENSP00000434586.1:p.Asp4605Tyr
ENST00000589042.5:c.41008G>T MANE Select	ENSP00000467141.1:p.Asp13670Tyr
ENST00000591111.5:c.36085G>T	ENSP00000465570.1:p.Asp12029Tyr
ENST00000615779.4:c.36085G>T	ENSP00000483597.1:p.Asp12029Tyr
NM_001256850.1:c.36085G>T	NP_001243779.1:p.Asp12029Tyr
NM_001267550.2:c.41008G>T MANE Select	NP_001254479.2:p.Asp13670Tyr
NM_003319.4:c.13813G>T	NP_003310.4:p.Asp4605Tyr
NM_133378.4:c.33304G>T	NP_596869.4:p.Asp11102Tyr
NM_133432.3:c.14188G>T	NP_597676.3:p.Asp4730Tyr
NM_133437.4:c.14389G>T	NP_597681.4:p.Asp4797Tyr
XM_011511729.1:c.40105G>T	XP_011510031.1:p.Asp13369Tyr
XM_011511730.1:c.13999G>T	XP_011510032.1:p.Asp4667Tyr
XM_011511731.1:c.13858G>T	XP_011510033.1:p.Asp4620Tyr
XM_017004819.1:c.39901G>T	XP_016860308.1:p.Asp13301Tyr
XM_017004820.1:c.35299G>T	XP_016860309.1:p.Asp11767Tyr
XM_017004821.1:c.35296G>T	XP_016860310.1:p.Asp11766Tyr
XM_017004822.1:c.32338G>T	XP_016860311.1:p.Asp10780Tyr
XM_017004823.1:c.13954G>T	XP_016860312.1:p.Asp4652Tyr
XM_024453094.1:c.35449G>T	XP_024308862.1:p.Asp11817Tyr
XM_024453095.1:c.35446G>T	XP_024308863.1:p.Asp11816Tyr
XM_024453096.1:c.34879G>T	XP_024308864.1:p.Asp11627Tyr
XM_024453097.1:c.32221G>T	XP_024308865.1:p.Asp10741Tyr
XM_024453098.1:c.32140G>T	XP_024308866.1:p.Asp10714Tyr
XM_024453099.1:c.13903G>T	XP_024308867.1:p.Asp4635Tyr
XM_024453100.1:c.3757G>T	XP_024308868.1:p.Asp1253Tyr