Canonical Allele Identifier: CA349500061

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179457941G>T (hg19) ; chr2:g.178593214G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178593214G>T , CM000664.2:g.178593214G>T	GRCh38
NC_000002.11:g.179457941G>T , CM000664.1:g.179457941G>T	GRCh37
NC_000002.10:g.179166187G>T	NCBI36
NG_011618.3:g.242589C>A , LRG_391:g.242589C>A
NG_051363.1:g.75388G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51290C>A (TTN)	ENSP00000343764.6:p.Pro17097Gln
ENST00000342175.11:c.32375C>A (TTN)	ENSP00000340554.6:p.Pro10792Gln
ENST00000359218.10:c.32174C>A (TTN)	ENSP00000352154.5:p.Pro10725Gln
ENST00000342175.10:c.32375C>A (TTN)	ENSP00000340554.6:p.Pro10792Gln
ENST00000342992.10:c.51290C>A (TTN)	ENSP00000343764.6:p.Pro17097Gln
ENST00000359218.9:c.32174C>A (TTN)	ENSP00000352154.5:p.Pro10725Gln
ENST00000460472.6:c.31799C>A (TTN)	ENSP00000434586.1:p.Pro10600Gln
ENST00000589042.5:c.58994C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro19665Gln
ENST00000591111.5:c.54071C>A (TTN)	ENSP00000465570.1:p.Pro18024Gln
ENST00000615779.4:c.54071C>A (TTN)	ENSP00000483597.1:p.Pro18024Gln
NM_001256850.1:c.54071C>A (TTN)	NP_001243779.1:p.Pro18024Gln
NM_001267550.2:c.58994C>A (TTN) MANE Select	NP_001254479.2:p.Pro19665Gln
NM_003319.4:c.31799C>A (TTN)	NP_003310.4:p.Pro10600Gln
NM_133378.4:c.51290C>A (TTN)	NP_596869.4:p.Pro17097Gln
NM_133432.3:c.32174C>A (TTN)	NP_597676.3:p.Pro10725Gln
NM_133437.4:c.32375C>A (TTN)	NP_597681.4:p.Pro10792Gln
NR_038271.1:n.597-4382G>T (TTN-AS1)
NR_038272.1:n.3364+1900G>T (TTN-AS1)
XM_011511729.1:c.58091C>A (TTN)	XP_011510031.1:p.Pro19364Gln
XM_011511730.1:c.31985C>A (TTN)	XP_011510032.1:p.Pro10662Gln
XM_011511731.1:c.31844C>A (TTN)	XP_011510033.1:p.Pro10615Gln
XM_017004819.1:c.57887C>A (TTN)	XP_016860308.1:p.Pro19296Gln
XM_017004820.1:c.53285C>A (TTN)	XP_016860309.1:p.Pro17762Gln
XM_017004821.1:c.53282C>A (TTN)	XP_016860310.1:p.Pro17761Gln
XM_017004822.1:c.50324C>A (TTN)	XP_016860311.1:p.Pro16775Gln
XM_017004823.1:c.31940C>A (TTN)	XP_016860312.1:p.Pro10647Gln
XM_024453094.1:c.53435C>A (TTN)	XP_024308862.1:p.Pro17812Gln
XM_024453095.1:c.53432C>A (TTN)	XP_024308863.1:p.Pro17811Gln
XM_024453096.1:c.52865C>A (TTN)	XP_024308864.1:p.Pro17622Gln
XM_024453097.1:c.50207C>A (TTN)	XP_024308865.1:p.Pro16736Gln
XM_024453098.1:c.50126C>A (TTN)	XP_024308866.1:p.Pro16709Gln
XM_024453099.1:c.31889C>A (TTN)	XP_024308867.1:p.Pro10630Gln
XM_024453100.1:c.21743C>A (TTN)	XP_024308868.1:p.Pro7248Gln