Canonical Allele Identifier: CA349591784

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179476106G>C (hg19) ; chr2:g.178611379G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178611379G>C , CM000664.2:g.178611379G>C	GRCh38
NC_000002.11:g.179476106G>C , CM000664.1:g.179476106G>C	GRCh37
NC_000002.10:g.179184351G>C	NCBI36
NG_011618.3:g.224424C>G , LRG_391:g.224424C>G
NG_051363.1:g.93553G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.43146C>G (TTN)	ENSP00000343764.6:p.Asp14382Glu
ENST00000342175.11:c.24231C>G (TTN)	ENSP00000340554.6:p.Asp8077Glu
ENST00000359218.10:c.24030C>G (TTN)	ENSP00000352154.5:p.Asp8010Glu
ENST00000342175.10:c.24231C>G (TTN)	ENSP00000340554.6:p.Asp8077Glu
ENST00000342992.10:c.43146C>G (TTN)	ENSP00000343764.6:p.Asp14382Glu
ENST00000359218.9:c.24030C>G (TTN)	ENSP00000352154.5:p.Asp8010Glu
ENST00000460472.6:c.23655C>G (TTN)	ENSP00000434586.1:p.Asp7885Glu
ENST00000589042.5:c.50850C>G (TTN) MANE Select	ENSP00000467141.1:p.Asp16950Glu
ENST00000591111.5:c.45927C>G (TTN)	ENSP00000465570.1:p.Asp15309Glu
ENST00000615779.4:c.45927C>G (TTN)	ENSP00000483597.1:p.Asp15309Glu
NM_001256850.1:c.45927C>G (TTN)	NP_001243779.1:p.Asp15309Glu
NM_001267550.2:c.50850C>G (TTN) MANE Select	NP_001254479.2:p.Asp16950Glu
NM_003319.4:c.23655C>G (TTN)	NP_003310.4:p.Asp7885Glu
NM_133378.4:c.43146C>G (TTN)	NP_596869.4:p.Asp14382Glu
NM_133432.3:c.24030C>G (TTN)	NP_597676.3:p.Asp8010Glu
NM_133437.4:c.24231C>G (TTN)	NP_597681.4:p.Asp8077Glu
NR_038271.1:n.783-2656G>C (TTN-AS1)
XM_011511729.1:c.49947C>G (TTN)	XP_011510031.1:p.Asp16649Glu
XM_011511730.1:c.23841C>G (TTN)	XP_011510032.1:p.Asp7947Glu
XM_011511731.1:c.23700C>G (TTN)	XP_011510033.1:p.Asp7900Glu
XM_017004819.1:c.49743C>G (TTN)	XP_016860308.1:p.Asp16581Glu
XM_017004820.1:c.45141C>G (TTN)	XP_016860309.1:p.Asp15047Glu
XM_017004821.1:c.45138C>G (TTN)	XP_016860310.1:p.Asp15046Glu
XM_017004822.1:c.42180C>G (TTN)	XP_016860311.1:p.Asp14060Glu
XM_017004823.1:c.23796C>G (TTN)	XP_016860312.1:p.Asp7932Glu
XM_024453094.1:c.45291C>G (TTN)	XP_024308862.1:p.Asp15097Glu
XM_024453095.1:c.45288C>G (TTN)	XP_024308863.1:p.Asp15096Glu
XM_024453096.1:c.44721C>G (TTN)	XP_024308864.1:p.Asp14907Glu
XM_024453097.1:c.42063C>G (TTN)	XP_024308865.1:p.Asp14021Glu
XM_024453098.1:c.41982C>G (TTN)	XP_024308866.1:p.Asp13994Glu
XM_024453099.1:c.23745C>G (TTN)	XP_024308867.1:p.Asp7915Glu
XM_024453100.1:c.13599C>G (TTN)	XP_024308868.1:p.Asp4533Glu