Canonical Allele Identifier: CA349670828

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577399G>T , CM000664.2:g.178577399G>T	GRCh38
NC_000002.11:g.179442126G>T , CM000664.1:g.179442126G>T	GRCh37
NC_000002.10:g.179150372G>T	NCBI36
NG_011618.3:g.258404C>A , LRG_391:g.258404C>A
NG_051363.1:g.59573G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.68936C>A (TTN) MANE Select	NP_001254479.2:p.Ser22979Ter
ENST00000589042.5:c.68936C>A (TTN) MANE Select	ENSP00000467141.1:p.Ser22979Ter
NM_001256850.1:c.64013C>A (TTN)	NP_001243779.1:p.Ser21338Ter
NM_003319.4:c.41741C>A (TTN)	NP_003310.4:p.Ser13914Ter
NM_133378.4:c.61232C>A (TTN)	NP_596869.4:p.Ser20411Ter
NM_133432.3:c.42116C>A (TTN)	NP_597676.3:p.Ser14039Ter
NM_133437.4:c.42317C>A (TTN)	NP_597681.4:p.Ser14106Ter
NR_038271.1:n.596+5950G>T (TTN-AS1)
NR_038272.1:n.2044-5173G>T (TTN-AS1)
ENST00000342175.10:c.42317C>A (TTN)	ENSP00000340554.6:p.Ser14106Ter
ENST00000342175.11:c.42317C>A (TTN)	ENSP00000340554.6:p.Ser14106Ter
ENST00000342992.10:c.61232C>A (TTN)	ENSP00000343764.6:p.Ser20411Ter
ENST00000342992.11:c.61232C>A (TTN)	ENSP00000343764.6:p.Ser20411Ter
ENST00000359218.10:c.42116C>A (TTN)	ENSP00000352154.5:p.Ser14039Ter
ENST00000359218.9:c.42116C>A (TTN)	ENSP00000352154.5:p.Ser14039Ter
ENST00000460472.6:c.41741C>A (TTN)	ENSP00000434586.1:p.Ser13914Ter
ENST00000591111.5:c.64013C>A (TTN)	ENSP00000465570.1:p.Ser21338Ter
ENST00000615779.4:c.64013C>A (TTN)	ENSP00000483597.1:p.Ser21338Ter
XM_011511729.1:c.68033C>A (TTN)	XP_011510031.1:p.Ser22678Ter
XM_011511730.1:c.41927C>A (TTN)	XP_011510032.1:p.Ser13976Ter
XM_011511731.1:c.41786C>A (TTN)	XP_011510033.1:p.Ser13929Ter
XM_017004819.1:c.67829C>A (TTN)	XP_016860308.1:p.Ser22610Ter
XM_017004820.1:c.63227C>A (TTN)	XP_016860309.1:p.Ser21076Ter
XM_017004821.1:c.63224C>A (TTN)	XP_016860310.1:p.Ser21075Ter
XM_017004822.1:c.60266C>A (TTN)	XP_016860311.1:p.Ser20089Ter
XM_017004823.1:c.41882C>A (TTN)	XP_016860312.1:p.Ser13961Ter
XM_024453094.1:c.63377C>A (TTN)	XP_024308862.1:p.Ser21126Ter
XM_024453095.1:c.63374C>A (TTN)	XP_024308863.1:p.Ser21125Ter
XM_024453096.1:c.62807C>A (TTN)	XP_024308864.1:p.Ser20936Ter
XM_024453097.1:c.60149C>A (TTN)	XP_024308865.1:p.Ser20050Ter
XM_024453098.1:c.60068C>A (TTN)	XP_024308866.1:p.Ser20023Ter
XM_024453099.1:c.41831C>A (TTN)	XP_024308867.1:p.Ser13944Ter
XM_024453100.1:c.31685C>A (TTN)	XP_024308868.1:p.Ser10562Ter