Canonical Allele Identifier: CA349618794

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482942T>G (hg19) ; chr2:g.178618215T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618215T>G , CM000664.2:g.178618215T>G	GRCh38
NC_000002.11:g.179482942T>G , CM000664.1:g.179482942T>G	GRCh37
NC_000002.10:g.179191187T>G	NCBI36
NG_011618.3:g.217588A>C , LRG_391:g.217588A>C
NG_051363.1:g.100389T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39539A>C (TTN)	ENSP00000343764.6:p.Asn13180Thr
ENST00000342175.11:c.20624A>C (TTN)	ENSP00000340554.6:p.Asn6875Thr
ENST00000359218.10:c.20423A>C (TTN)	ENSP00000352154.5:p.Asn6808Thr
ENST00000342175.10:c.20624A>C (TTN)	ENSP00000340554.6:p.Asn6875Thr
ENST00000342992.10:c.39539A>C (TTN)	ENSP00000343764.6:p.Asn13180Thr
ENST00000359218.9:c.20423A>C (TTN)	ENSP00000352154.5:p.Asn6808Thr
ENST00000460472.6:c.20048A>C (TTN)	ENSP00000434586.1:p.Asn6683Thr
ENST00000589042.5:c.47243A>C (TTN) MANE Select	ENSP00000467141.1:p.Asn15748Thr
ENST00000591111.5:c.42320A>C (TTN)	ENSP00000465570.1:p.Asn14107Thr
ENST00000615779.4:c.42320A>C (TTN)	ENSP00000483597.1:p.Asn14107Thr
NM_001256850.1:c.42320A>C (TTN)	NP_001243779.1:p.Asn14107Thr
NM_001267550.2:c.47243A>C (TTN) MANE Select	NP_001254479.2:p.Asn15748Thr
NM_003319.4:c.20048A>C (TTN)	NP_003310.4:p.Asn6683Thr
NM_133378.4:c.39539A>C (TTN)	NP_596869.4:p.Asn13180Thr
NM_133432.3:c.20423A>C (TTN)	NP_597676.3:p.Asn6808Thr
NM_133437.4:c.20624A>C (TTN)	NP_597681.4:p.Asn6875Thr
NR_038271.1:n.1605-1538T>G (TTN-AS1)
XM_011511729.1:c.46340A>C (TTN)	XP_011510031.1:p.Asn15447Thr
XM_011511730.1:c.20234A>C (TTN)	XP_011510032.1:p.Asn6745Thr
XM_011511731.1:c.20093A>C (TTN)	XP_011510033.1:p.Asn6698Thr
XM_017004819.1:c.46136A>C (TTN)	XP_016860308.1:p.Asn15379Thr
XM_017004820.1:c.41534A>C (TTN)	XP_016860309.1:p.Asn13845Thr
XM_017004821.1:c.41531A>C (TTN)	XP_016860310.1:p.Asn13844Thr
XM_017004822.1:c.38573A>C (TTN)	XP_016860311.1:p.Asn12858Thr
XM_017004823.1:c.20189A>C (TTN)	XP_016860312.1:p.Asn6730Thr
XM_024453094.1:c.41684A>C (TTN)	XP_024308862.1:p.Asn13895Thr
XM_024453095.1:c.41681A>C (TTN)	XP_024308863.1:p.Asn13894Thr
XM_024453096.1:c.41114A>C (TTN)	XP_024308864.1:p.Asn13705Thr
XM_024453097.1:c.38456A>C (TTN)	XP_024308865.1:p.Asn12819Thr
XM_024453098.1:c.38375A>C (TTN)	XP_024308866.1:p.Asn12792Thr
XM_024453099.1:c.20138A>C (TTN)	XP_024308867.1:p.Asn6713Thr
XM_024453100.1:c.9992A>C (TTN)	XP_024308868.1:p.Asn3331Thr