Canonical Allele Identifier: CA349495770

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414524T>C (hg19) ; chr2:g.178549797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549797T>C , CM000664.2:g.178549797T>C	GRCh38
NC_000002.11:g.179414524T>C , CM000664.1:g.179414524T>C	GRCh37
NC_000002.10:g.179122770T>C	NCBI36
NG_011618.3:g.286006A>G , LRG_391:g.286006A>G
NG_051363.1:g.31971T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84221A>G (TTN)	ENSP00000343764.6:p.Asp28074Gly
ENST00000342175.11:c.65306A>G (TTN)	ENSP00000340554.6:p.Asp21769Gly
ENST00000359218.10:c.65105A>G (TTN)	ENSP00000352154.5:p.Asp21702Gly
ENST00000342175.10:c.65306A>G (TTN)	ENSP00000340554.6:p.Asp21769Gly
ENST00000342992.10:c.84221A>G (TTN)	ENSP00000343764.6:p.Asp28074Gly
ENST00000359218.9:c.65105A>G (TTN)	ENSP00000352154.5:p.Asp21702Gly
ENST00000460472.6:c.64730A>G (TTN)	ENSP00000434586.1:p.Asp21577Gly
ENST00000589042.5:c.91925A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp30642Gly
ENST00000591111.5:c.87002A>G (TTN)	ENSP00000465570.1:p.Asp29001Gly
ENST00000615779.4:c.87002A>G (TTN)	ENSP00000483597.1:p.Asp29001Gly
NM_001256850.1:c.87002A>G (TTN)	NP_001243779.1:p.Asp29001Gly
NM_001267550.2:c.91925A>G (TTN) MANE Select	NP_001254479.2:p.Asp30642Gly
NM_003319.4:c.64730A>G (TTN)	NP_003310.4:p.Asp21577Gly
NM_133378.4:c.84221A>G (TTN)	NP_596869.4:p.Asp28074Gly
NM_133432.3:c.65105A>G (TTN)	NP_597676.3:p.Asp21702Gly
NM_133437.4:c.65306A>G (TTN)	NP_597681.4:p.Asp21769Gly
NR_038271.1:n.447-21503T>C (TTN-AS1)
NR_038272.1:n.2043+7436T>C (TTN-AS1)
XM_011511729.1:c.91022A>G (TTN)	XP_011510031.1:p.Asp30341Gly
XM_011511730.1:c.64916A>G (TTN)	XP_011510032.1:p.Asp21639Gly
XM_011511731.1:c.64775A>G (TTN)	XP_011510033.1:p.Asp21592Gly
XM_017004819.1:c.90818A>G (TTN)	XP_016860308.1:p.Asp30273Gly
XM_017004820.1:c.86216A>G (TTN)	XP_016860309.1:p.Asp28739Gly
XM_017004821.1:c.86213A>G (TTN)	XP_016860310.1:p.Asp28738Gly
XM_017004822.1:c.83255A>G (TTN)	XP_016860311.1:p.Asp27752Gly
XM_017004823.1:c.64871A>G (TTN)	XP_016860312.1:p.Asp21624Gly
XM_024453094.1:c.86366A>G (TTN)	XP_024308862.1:p.Asp28789Gly
XM_024453095.1:c.86363A>G (TTN)	XP_024308863.1:p.Asp28788Gly
XM_024453096.1:c.85796A>G (TTN)	XP_024308864.1:p.Asp28599Gly
XM_024453097.1:c.83138A>G (TTN)	XP_024308865.1:p.Asp27713Gly
XM_024453098.1:c.83057A>G (TTN)	XP_024308866.1:p.Asp27686Gly
XM_024453099.1:c.64820A>G (TTN)	XP_024308867.1:p.Asp21607Gly
XM_024453100.1:c.54674A>G (TTN)	XP_024308868.1:p.Asp18225Gly