Canonical Allele Identifier: CA349661957

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501497C>G (hg19) ; chr2:g.178636770C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636770C>G , CM000664.2:g.178636770C>G	GRCh38
NC_000002.11:g.179501497C>G , CM000664.1:g.179501497C>G	GRCh37
NC_000002.10:g.179209742C>G	NCBI36
NG_011618.3:g.199033G>C , LRG_391:g.199033G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33253G>C	ENSP00000343764.6:p.Glu11085Gln
ENST00000342175.11:c.14338G>C	ENSP00000340554.6:p.Glu4780Gln
ENST00000359218.10:c.14137G>C	ENSP00000352154.5:p.Glu4713Gln
ENST00000342175.10:c.14338G>C	ENSP00000340554.6:p.Glu4780Gln
ENST00000342992.10:c.33253G>C	ENSP00000343764.6:p.Glu11085Gln
ENST00000359218.9:c.14137G>C	ENSP00000352154.5:p.Glu4713Gln
ENST00000414766.5:c.2869G>C	ENSP00000401501.1:p.Glu957Gln
ENST00000460472.6:c.13762G>C	ENSP00000434586.1:p.Glu4588Gln
ENST00000589042.5:c.40957G>C MANE Select	ENSP00000467141.1:p.Glu13653Gln
ENST00000591111.5:c.36034G>C	ENSP00000465570.1:p.Glu12012Gln
ENST00000615779.4:c.36034G>C	ENSP00000483597.1:p.Glu12012Gln
NM_001256850.1:c.36034G>C	NP_001243779.1:p.Glu12012Gln
NM_001267550.2:c.40957G>C MANE Select	NP_001254479.2:p.Glu13653Gln
NM_003319.4:c.13762G>C	NP_003310.4:p.Glu4588Gln
NM_133378.4:c.33253G>C	NP_596869.4:p.Glu11085Gln
NM_133432.3:c.14137G>C	NP_597676.3:p.Glu4713Gln
NM_133437.4:c.14338G>C	NP_597681.4:p.Glu4780Gln
XM_011511729.1:c.40054G>C	XP_011510031.1:p.Glu13352Gln
XM_011511730.1:c.13948G>C	XP_011510032.1:p.Glu4650Gln
XM_011511731.1:c.13807G>C	XP_011510033.1:p.Glu4603Gln
XM_017004819.1:c.39850G>C	XP_016860308.1:p.Glu13284Gln
XM_017004820.1:c.35248G>C	XP_016860309.1:p.Glu11750Gln
XM_017004821.1:c.35245G>C	XP_016860310.1:p.Glu11749Gln
XM_017004822.1:c.32287G>C	XP_016860311.1:p.Glu10763Gln
XM_017004823.1:c.13903G>C	XP_016860312.1:p.Glu4635Gln
XM_024453094.1:c.35398G>C	XP_024308862.1:p.Glu11800Gln
XM_024453095.1:c.35395G>C	XP_024308863.1:p.Glu11799Gln
XM_024453096.1:c.34828G>C	XP_024308864.1:p.Glu11610Gln
XM_024453097.1:c.32170G>C	XP_024308865.1:p.Glu10724Gln
XM_024453098.1:c.32089G>C	XP_024308866.1:p.Glu10697Gln
XM_024453099.1:c.13852G>C	XP_024308867.1:p.Glu4618Gln
XM_024453100.1:c.3706G>C	XP_024308868.1:p.Glu1236Gln