Canonical Allele Identifier: CA349604968

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179478650G>T (hg19) ; chr2:g.178613923G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178613923G>T , CM000664.2:g.178613923G>T	GRCh38
NC_000002.11:g.179478650G>T , CM000664.1:g.179478650G>T	GRCh37
NC_000002.10:g.179186895G>T	NCBI36
NG_011618.3:g.221880C>A , LRG_391:g.221880C>A
NG_051363.1:g.96097G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.41656C>A (TTN)	ENSP00000343764.6:p.Pro13886Thr
ENST00000342175.11:c.22741C>A (TTN)	ENSP00000340554.6:p.Pro7581Thr
ENST00000359218.10:c.22540C>A (TTN)	ENSP00000352154.5:p.Pro7514Thr
ENST00000342175.10:c.22741C>A (TTN)	ENSP00000340554.6:p.Pro7581Thr
ENST00000342992.10:c.41656C>A (TTN)	ENSP00000343764.6:p.Pro13886Thr
ENST00000359218.9:c.22540C>A (TTN)	ENSP00000352154.5:p.Pro7514Thr
ENST00000460472.6:c.22165C>A (TTN)	ENSP00000434586.1:p.Pro7389Thr
ENST00000589042.5:c.49360C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro16454Thr
ENST00000591111.5:c.44437C>A (TTN)	ENSP00000465570.1:p.Pro14813Thr
ENST00000615779.4:c.44437C>A (TTN)	ENSP00000483597.1:p.Pro14813Thr
NM_001256850.1:c.44437C>A (TTN)	NP_001243779.1:p.Pro14813Thr
NM_001267550.2:c.49360C>A (TTN) MANE Select	NP_001254479.2:p.Pro16454Thr
NM_003319.4:c.22165C>A (TTN)	NP_003310.4:p.Pro7389Thr
NM_133378.4:c.41656C>A (TTN)	NP_596869.4:p.Pro13886Thr
NM_133432.3:c.22540C>A (TTN)	NP_597676.3:p.Pro7514Thr
NM_133437.4:c.22741C>A (TTN)	NP_597681.4:p.Pro7581Thr
NR_038271.1:n.783-112G>T (TTN-AS1)
XM_011511729.1:c.48457C>A (TTN)	XP_011510031.1:p.Pro16153Thr
XM_011511730.1:c.22351C>A (TTN)	XP_011510032.1:p.Pro7451Thr
XM_011511731.1:c.22210C>A (TTN)	XP_011510033.1:p.Pro7404Thr
XM_017004819.1:c.48253C>A (TTN)	XP_016860308.1:p.Pro16085Thr
XM_017004820.1:c.43651C>A (TTN)	XP_016860309.1:p.Pro14551Thr
XM_017004821.1:c.43648C>A (TTN)	XP_016860310.1:p.Pro14550Thr
XM_017004822.1:c.40690C>A (TTN)	XP_016860311.1:p.Pro13564Thr
XM_017004823.1:c.22306C>A (TTN)	XP_016860312.1:p.Pro7436Thr
XM_024453094.1:c.43801C>A (TTN)	XP_024308862.1:p.Pro14601Thr
XM_024453095.1:c.43798C>A (TTN)	XP_024308863.1:p.Pro14600Thr
XM_024453096.1:c.43231C>A (TTN)	XP_024308864.1:p.Pro14411Thr
XM_024453097.1:c.40573C>A (TTN)	XP_024308865.1:p.Pro13525Thr
XM_024453098.1:c.40492C>A (TTN)	XP_024308866.1:p.Pro13498Thr
XM_024453099.1:c.22255C>A (TTN)	XP_024308867.1:p.Pro7419Thr
XM_024453100.1:c.12109C>A (TTN)	XP_024308868.1:p.Pro4037Thr