Canonical Allele Identifier: CA349400210

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179392336A>T (hg19) ; chr2:g.178527609A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527609A>T , CM000664.2:g.178527609A>T	GRCh38
NC_000002.11:g.179392336A>T , CM000664.1:g.179392336A>T	GRCh37
NC_000002.10:g.179100582A>T	NCBI36
NG_011618.3:g.308194T>A , LRG_391:g.308194T>A
NG_051363.1:g.9783A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99813T>A (TTN)	ENSP00000343764.6:p.Ser33271Arg
ENST00000342175.11:c.80898T>A (TTN)	ENSP00000340554.6:p.Ser26966Arg
ENST00000359218.10:c.80697T>A (TTN)	ENSP00000352154.5:p.Ser26899Arg
ENST00000342175.10:c.80898T>A (TTN)	ENSP00000340554.6:p.Ser26966Arg
ENST00000342992.10:c.99813T>A (TTN)	ENSP00000343764.6:p.Ser33271Arg
ENST00000359218.9:c.80697T>A (TTN)	ENSP00000352154.5:p.Ser26899Arg
ENST00000460472.6:c.80322T>A (TTN)	ENSP00000434586.1:p.Ser26774Arg
ENST00000589042.5:c.107517T>A (TTN) MANE Select	ENSP00000467141.1:p.Ser35839Arg
ENST00000591111.5:c.102594T>A (TTN)	ENSP00000465570.1:p.Ser34198Arg
ENST00000615779.4:c.102594T>A (TTN)	ENSP00000483597.1:p.Ser34198Arg
NM_001256850.1:c.102594T>A (TTN)	NP_001243779.1:p.Ser34198Arg
NM_001267550.2:c.107517T>A (TTN) MANE Select	NP_001254479.2:p.Ser35839Arg
NM_003319.4:c.80322T>A (TTN)	NP_003310.4:p.Ser26774Arg
NM_133378.4:c.99813T>A (TTN)	NP_596869.4:p.Ser33271Arg
NM_133432.3:c.80697T>A (TTN)	NP_597676.3:p.Ser26899Arg
NM_133437.4:c.80898T>A (TTN)	NP_597681.4:p.Ser26966Arg
NR_038271.1:n.446+3973A>T (TTN-AS1)
NR_038272.1:n.219+3973A>T (TTN-AS1)
XM_011511729.1:c.106614T>A (TTN)	XP_011510031.1:p.Ser35538Arg
XM_011511730.1:c.80508T>A (TTN)	XP_011510032.1:p.Ser26836Arg
XM_011511731.1:c.80367T>A (TTN)	XP_011510033.1:p.Ser26789Arg
XM_017004819.1:c.106410T>A (TTN)	XP_016860308.1:p.Ser35470Arg
XM_017004820.1:c.101808T>A (TTN)	XP_016860309.1:p.Ser33936Arg
XM_017004821.1:c.101805T>A (TTN)	XP_016860310.1:p.Ser33935Arg
XM_017004822.1:c.98847T>A (TTN)	XP_016860311.1:p.Ser32949Arg
XM_017004823.1:c.80463T>A (TTN)	XP_016860312.1:p.Ser26821Arg
XM_024453094.1:c.101958T>A (TTN)	XP_024308862.1:p.Ser33986Arg
XM_024453095.1:c.101955T>A (TTN)	XP_024308863.1:p.Ser33985Arg
XM_024453096.1:c.101388T>A (TTN)	XP_024308864.1:p.Ser33796Arg
XM_024453097.1:c.98730T>A (TTN)	XP_024308865.1:p.Ser32910Arg
XM_024453098.1:c.98649T>A (TTN)	XP_024308866.1:p.Ser32883Arg
XM_024453099.1:c.80412T>A (TTN)	XP_024308867.1:p.Ser26804Arg
XM_024453100.1:c.70266T>A (TTN)	XP_024308868.1:p.Ser23422Arg