Canonical Allele Identifier: CA349618778

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482940G>T (hg19) ; chr2:g.178618213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618213G>T , CM000664.2:g.178618213G>T	GRCh38
NC_000002.11:g.179482940G>T , CM000664.1:g.179482940G>T	GRCh37
NC_000002.10:g.179191185G>T	NCBI36
NG_011618.3:g.217590C>A , LRG_391:g.217590C>A
NG_051363.1:g.100387G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39541C>A (TTN)	ENSP00000343764.6:p.Pro13181Thr
ENST00000342175.11:c.20626C>A (TTN)	ENSP00000340554.6:p.Pro6876Thr
ENST00000359218.10:c.20425C>A (TTN)	ENSP00000352154.5:p.Pro6809Thr
ENST00000342175.10:c.20626C>A (TTN)	ENSP00000340554.6:p.Pro6876Thr
ENST00000342992.10:c.39541C>A (TTN)	ENSP00000343764.6:p.Pro13181Thr
ENST00000359218.9:c.20425C>A (TTN)	ENSP00000352154.5:p.Pro6809Thr
ENST00000460472.6:c.20050C>A (TTN)	ENSP00000434586.1:p.Pro6684Thr
ENST00000589042.5:c.47245C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro15749Thr
ENST00000591111.5:c.42322C>A (TTN)	ENSP00000465570.1:p.Pro14108Thr
ENST00000615779.4:c.42322C>A (TTN)	ENSP00000483597.1:p.Pro14108Thr
NM_001256850.1:c.42322C>A (TTN)	NP_001243779.1:p.Pro14108Thr
NM_001267550.2:c.47245C>A (TTN) MANE Select	NP_001254479.2:p.Pro15749Thr
NM_003319.4:c.20050C>A (TTN)	NP_003310.4:p.Pro6684Thr
NM_133378.4:c.39541C>A (TTN)	NP_596869.4:p.Pro13181Thr
NM_133432.3:c.20425C>A (TTN)	NP_597676.3:p.Pro6809Thr
NM_133437.4:c.20626C>A (TTN)	NP_597681.4:p.Pro6876Thr
NR_038271.1:n.1605-1540G>T (TTN-AS1)
XM_011511729.1:c.46342C>A (TTN)	XP_011510031.1:p.Pro15448Thr
XM_011511730.1:c.20236C>A (TTN)	XP_011510032.1:p.Pro6746Thr
XM_011511731.1:c.20095C>A (TTN)	XP_011510033.1:p.Pro6699Thr
XM_017004819.1:c.46138C>A (TTN)	XP_016860308.1:p.Pro15380Thr
XM_017004820.1:c.41536C>A (TTN)	XP_016860309.1:p.Pro13846Thr
XM_017004821.1:c.41533C>A (TTN)	XP_016860310.1:p.Pro13845Thr
XM_017004822.1:c.38575C>A (TTN)	XP_016860311.1:p.Pro12859Thr
XM_017004823.1:c.20191C>A (TTN)	XP_016860312.1:p.Pro6731Thr
XM_024453094.1:c.41686C>A (TTN)	XP_024308862.1:p.Pro13896Thr
XM_024453095.1:c.41683C>A (TTN)	XP_024308863.1:p.Pro13895Thr
XM_024453096.1:c.41116C>A (TTN)	XP_024308864.1:p.Pro13706Thr
XM_024453097.1:c.38458C>A (TTN)	XP_024308865.1:p.Pro12820Thr
XM_024453098.1:c.38377C>A (TTN)	XP_024308866.1:p.Pro12793Thr
XM_024453099.1:c.20140C>A (TTN)	XP_024308867.1:p.Pro6714Thr
XM_024453100.1:c.9994C>A (TTN)	XP_024308868.1:p.Pro3332Thr