Canonical Allele Identifier: CA349496185

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414561T>G (hg19) ; chr2:g.178549834T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549834T>G , CM000664.2:g.178549834T>G	GRCh38
NC_000002.11:g.179414561T>G , CM000664.1:g.179414561T>G	GRCh37
NC_000002.10:g.179122807T>G	NCBI36
NG_011618.3:g.285969A>C , LRG_391:g.285969A>C
NG_051363.1:g.32008T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84184A>C (TTN)	ENSP00000343764.6:p.Thr28062Pro
ENST00000342175.11:c.65269A>C (TTN)	ENSP00000340554.6:p.Thr21757Pro
ENST00000359218.10:c.65068A>C (TTN)	ENSP00000352154.5:p.Thr21690Pro
ENST00000342175.10:c.65269A>C (TTN)	ENSP00000340554.6:p.Thr21757Pro
ENST00000342992.10:c.84184A>C (TTN)	ENSP00000343764.6:p.Thr28062Pro
ENST00000359218.9:c.65068A>C (TTN)	ENSP00000352154.5:p.Thr21690Pro
ENST00000460472.6:c.64693A>C (TTN)	ENSP00000434586.1:p.Thr21565Pro
ENST00000589042.5:c.91888A>C (TTN) MANE Select	ENSP00000467141.1:p.Thr30630Pro
ENST00000591111.5:c.86965A>C (TTN)	ENSP00000465570.1:p.Thr28989Pro
ENST00000615779.4:c.86965A>C (TTN)	ENSP00000483597.1:p.Thr28989Pro
NM_001256850.1:c.86965A>C (TTN)	NP_001243779.1:p.Thr28989Pro
NM_001267550.2:c.91888A>C (TTN) MANE Select	NP_001254479.2:p.Thr30630Pro
NM_003319.4:c.64693A>C (TTN)	NP_003310.4:p.Thr21565Pro
NM_133378.4:c.84184A>C (TTN)	NP_596869.4:p.Thr28062Pro
NM_133432.3:c.65068A>C (TTN)	NP_597676.3:p.Thr21690Pro
NM_133437.4:c.65269A>C (TTN)	NP_597681.4:p.Thr21757Pro
NR_038271.1:n.447-21466T>G (TTN-AS1)
NR_038272.1:n.2043+7473T>G (TTN-AS1)
XM_011511729.1:c.90985A>C (TTN)	XP_011510031.1:p.Thr30329Pro
XM_011511730.1:c.64879A>C (TTN)	XP_011510032.1:p.Thr21627Pro
XM_011511731.1:c.64738A>C (TTN)	XP_011510033.1:p.Thr21580Pro
XM_017004819.1:c.90781A>C (TTN)	XP_016860308.1:p.Thr30261Pro
XM_017004820.1:c.86179A>C (TTN)	XP_016860309.1:p.Thr28727Pro
XM_017004821.1:c.86176A>C (TTN)	XP_016860310.1:p.Thr28726Pro
XM_017004822.1:c.83218A>C (TTN)	XP_016860311.1:p.Thr27740Pro
XM_017004823.1:c.64834A>C (TTN)	XP_016860312.1:p.Thr21612Pro
XM_024453094.1:c.86329A>C (TTN)	XP_024308862.1:p.Thr28777Pro
XM_024453095.1:c.86326A>C (TTN)	XP_024308863.1:p.Thr28776Pro
XM_024453096.1:c.85759A>C (TTN)	XP_024308864.1:p.Thr28587Pro
XM_024453097.1:c.83101A>C (TTN)	XP_024308865.1:p.Thr27701Pro
XM_024453098.1:c.83020A>C (TTN)	XP_024308866.1:p.Thr27674Pro
XM_024453099.1:c.64783A>C (TTN)	XP_024308867.1:p.Thr21595Pro
XM_024453100.1:c.54637A>C (TTN)	XP_024308868.1:p.Thr18213Pro