Canonical Allele Identifier: CA349423100

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179444025G>T (hg19) ; chr2:g.178579298G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178579298G>T , CM000664.2:g.178579298G>T	GRCh38
NC_000002.11:g.179444025G>T , CM000664.1:g.179444025G>T	GRCh37
NC_000002.10:g.179152271G>T	NCBI36
NG_011618.3:g.256505C>A , LRG_391:g.256505C>A
NG_051363.1:g.61472G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.60028C>A (TTN)	ENSP00000343764.6:p.Pro20010Thr
ENST00000342175.11:c.41113C>A (TTN)	ENSP00000340554.6:p.Pro13705Thr
ENST00000359218.10:c.40912C>A (TTN)	ENSP00000352154.5:p.Pro13638Thr
ENST00000342175.10:c.41113C>A (TTN)	ENSP00000340554.6:p.Pro13705Thr
ENST00000342992.10:c.60028C>A (TTN)	ENSP00000343764.6:p.Pro20010Thr
ENST00000359218.9:c.40912C>A (TTN)	ENSP00000352154.5:p.Pro13638Thr
ENST00000460472.6:c.40537C>A (TTN)	ENSP00000434586.1:p.Pro13513Thr
ENST00000589042.5:c.67732C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro22578Thr
ENST00000591111.5:c.62809C>A (TTN)	ENSP00000465570.1:p.Pro20937Thr
ENST00000615779.4:c.62809C>A (TTN)	ENSP00000483597.1:p.Pro20937Thr
NM_001256850.1:c.62809C>A (TTN)	NP_001243779.1:p.Pro20937Thr
NM_001267550.2:c.67732C>A (TTN) MANE Select	NP_001254479.2:p.Pro22578Thr
NM_003319.4:c.40537C>A (TTN)	NP_003310.4:p.Pro13513Thr
NM_133378.4:c.60028C>A (TTN)	NP_596869.4:p.Pro20010Thr
NM_133432.3:c.40912C>A (TTN)	NP_597676.3:p.Pro13638Thr
NM_133437.4:c.41113C>A (TTN)	NP_597681.4:p.Pro13705Thr
NR_038271.1:n.596+7849G>T (TTN-AS1)
NR_038272.1:n.2044-3274G>T (TTN-AS1)
XM_011511729.1:c.66829C>A (TTN)	XP_011510031.1:p.Pro22277Thr
XM_011511730.1:c.40723C>A (TTN)	XP_011510032.1:p.Pro13575Thr
XM_011511731.1:c.40582C>A (TTN)	XP_011510033.1:p.Pro13528Thr
XM_017004819.1:c.66625C>A (TTN)	XP_016860308.1:p.Pro22209Thr
XM_017004820.1:c.62023C>A (TTN)	XP_016860309.1:p.Pro20675Thr
XM_017004821.1:c.62020C>A (TTN)	XP_016860310.1:p.Pro20674Thr
XM_017004822.1:c.59062C>A (TTN)	XP_016860311.1:p.Pro19688Thr
XM_017004823.1:c.40678C>A (TTN)	XP_016860312.1:p.Pro13560Thr
XM_024453094.1:c.62173C>A (TTN)	XP_024308862.1:p.Pro20725Thr
XM_024453095.1:c.62170C>A (TTN)	XP_024308863.1:p.Pro20724Thr
XM_024453096.1:c.61603C>A (TTN)	XP_024308864.1:p.Pro20535Thr
XM_024453097.1:c.58945C>A (TTN)	XP_024308865.1:p.Pro19649Thr
XM_024453098.1:c.58864C>A (TTN)	XP_024308866.1:p.Pro19622Thr
XM_024453099.1:c.40627C>A (TTN)	XP_024308867.1:p.Pro13543Thr
XM_024453100.1:c.30481C>A (TTN)	XP_024308868.1:p.Pro10161Thr