Canonical Allele Identifier: CA349661776

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501442T>G (hg19) ; chr2:g.178636715T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636715T>G , CM000664.2:g.178636715T>G	GRCh38
NC_000002.11:g.179501442T>G , CM000664.1:g.179501442T>G	GRCh37
NC_000002.10:g.179209687T>G	NCBI36
NG_011618.3:g.199088A>C , LRG_391:g.199088A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33308A>C	ENSP00000343764.6:p.Glu11103Ala
ENST00000342175.11:c.14393A>C	ENSP00000340554.6:p.Glu4798Ala
ENST00000359218.10:c.14192A>C	ENSP00000352154.5:p.Glu4731Ala
ENST00000342175.10:c.14393A>C	ENSP00000340554.6:p.Glu4798Ala
ENST00000342992.10:c.33308A>C	ENSP00000343764.6:p.Glu11103Ala
ENST00000359218.9:c.14192A>C	ENSP00000352154.5:p.Glu4731Ala
ENST00000460472.6:c.13817A>C	ENSP00000434586.1:p.Glu4606Ala
ENST00000589042.5:c.41012A>C MANE Select	ENSP00000467141.1:p.Glu13671Ala
ENST00000591111.5:c.36089A>C	ENSP00000465570.1:p.Glu12030Ala
ENST00000615779.4:c.36089A>C	ENSP00000483597.1:p.Glu12030Ala
NM_001256850.1:c.36089A>C	NP_001243779.1:p.Glu12030Ala
NM_001267550.2:c.41012A>C MANE Select	NP_001254479.2:p.Glu13671Ala
NM_003319.4:c.13817A>C	NP_003310.4:p.Glu4606Ala
NM_133378.4:c.33308A>C	NP_596869.4:p.Glu11103Ala
NM_133432.3:c.14192A>C	NP_597676.3:p.Glu4731Ala
NM_133437.4:c.14393A>C	NP_597681.4:p.Glu4798Ala
XM_011511729.1:c.40109A>C	XP_011510031.1:p.Glu13370Ala
XM_011511730.1:c.14003A>C	XP_011510032.1:p.Glu4668Ala
XM_011511731.1:c.13862A>C	XP_011510033.1:p.Glu4621Ala
XM_017004819.1:c.39905A>C	XP_016860308.1:p.Glu13302Ala
XM_017004820.1:c.35303A>C	XP_016860309.1:p.Glu11768Ala
XM_017004821.1:c.35300A>C	XP_016860310.1:p.Glu11767Ala
XM_017004822.1:c.32342A>C	XP_016860311.1:p.Glu10781Ala
XM_017004823.1:c.13958A>C	XP_016860312.1:p.Glu4653Ala
XM_024453094.1:c.35453A>C	XP_024308862.1:p.Glu11818Ala
XM_024453095.1:c.35450A>C	XP_024308863.1:p.Glu11817Ala
XM_024453096.1:c.34883A>C	XP_024308864.1:p.Glu11628Ala
XM_024453097.1:c.32225A>C	XP_024308865.1:p.Glu10742Ala
XM_024453098.1:c.32144A>C	XP_024308866.1:p.Glu10715Ala
XM_024453099.1:c.13907A>C	XP_024308867.1:p.Glu4636Ala
XM_024453100.1:c.3761A>C	XP_024308868.1:p.Glu1254Ala