Canonical Allele Identifier: CA349618850

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482952C>G (hg19) ; chr2:g.178618225C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618225C>G , CM000664.2:g.178618225C>G	GRCh38
NC_000002.11:g.179482952C>G , CM000664.1:g.179482952C>G	GRCh37
NC_000002.10:g.179191197C>G	NCBI36
NG_011618.3:g.217578G>C , LRG_391:g.217578G>C
NG_051363.1:g.100399C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39529G>C (TTN)	ENSP00000343764.6:p.Glu13177Gln
ENST00000342175.11:c.20614G>C (TTN)	ENSP00000340554.6:p.Glu6872Gln
ENST00000359218.10:c.20413G>C (TTN)	ENSP00000352154.5:p.Glu6805Gln
ENST00000342175.10:c.20614G>C (TTN)	ENSP00000340554.6:p.Glu6872Gln
ENST00000342992.10:c.39529G>C (TTN)	ENSP00000343764.6:p.Glu13177Gln
ENST00000359218.9:c.20413G>C (TTN)	ENSP00000352154.5:p.Glu6805Gln
ENST00000460472.6:c.20038G>C (TTN)	ENSP00000434586.1:p.Glu6680Gln
ENST00000589042.5:c.47233G>C (TTN) MANE Select	ENSP00000467141.1:p.Glu15745Gln
ENST00000591111.5:c.42310G>C (TTN)	ENSP00000465570.1:p.Glu14104Gln
ENST00000615779.4:c.42310G>C (TTN)	ENSP00000483597.1:p.Glu14104Gln
NM_001256850.1:c.42310G>C (TTN)	NP_001243779.1:p.Glu14104Gln
NM_001267550.2:c.47233G>C (TTN) MANE Select	NP_001254479.2:p.Glu15745Gln
NM_003319.4:c.20038G>C (TTN)	NP_003310.4:p.Glu6680Gln
NM_133378.4:c.39529G>C (TTN)	NP_596869.4:p.Glu13177Gln
NM_133432.3:c.20413G>C (TTN)	NP_597676.3:p.Glu6805Gln
NM_133437.4:c.20614G>C (TTN)	NP_597681.4:p.Glu6872Gln
NR_038271.1:n.1605-1528C>G (TTN-AS1)
XM_011511729.1:c.46330G>C (TTN)	XP_011510031.1:p.Glu15444Gln
XM_011511730.1:c.20224G>C (TTN)	XP_011510032.1:p.Glu6742Gln
XM_011511731.1:c.20083G>C (TTN)	XP_011510033.1:p.Glu6695Gln
XM_017004819.1:c.46126G>C (TTN)	XP_016860308.1:p.Glu15376Gln
XM_017004820.1:c.41524G>C (TTN)	XP_016860309.1:p.Glu13842Gln
XM_017004821.1:c.41521G>C (TTN)	XP_016860310.1:p.Glu13841Gln
XM_017004822.1:c.38563G>C (TTN)	XP_016860311.1:p.Glu12855Gln
XM_017004823.1:c.20179G>C (TTN)	XP_016860312.1:p.Glu6727Gln
XM_024453094.1:c.41674G>C (TTN)	XP_024308862.1:p.Glu13892Gln
XM_024453095.1:c.41671G>C (TTN)	XP_024308863.1:p.Glu13891Gln
XM_024453096.1:c.41104G>C (TTN)	XP_024308864.1:p.Glu13702Gln
XM_024453097.1:c.38446G>C (TTN)	XP_024308865.1:p.Glu12816Gln
XM_024453098.1:c.38365G>C (TTN)	XP_024308866.1:p.Glu12789Gln
XM_024453099.1:c.20128G>C (TTN)	XP_024308867.1:p.Glu6710Gln
XM_024453100.1:c.9982G>C (TTN)	XP_024308868.1:p.Glu3328Gln