Canonical Allele Identifier: CA430242528

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179411598T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546871T>A , CM000664.2:g.178546871T>A	GRCh38
NC_000002.11:g.179411598T>A , CM000664.1:g.179411598T>A	GRCh37
NC_000002.10:g.179119844T>A	NCBI36
NG_011618.3:g.288932A>T , LRG_391:g.288932A>T
NG_051363.1:g.29045T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86853A>T (TTN)	ENSP00000343764.6:p.Thr28951=
ENST00000342175.11:c.67938A>T (TTN)	ENSP00000340554.6:p.Thr22646=
ENST00000359218.10:c.67737A>T (TTN)	ENSP00000352154.5:p.Thr22579=
ENST00000342175.10:c.67938A>T (TTN)	ENSP00000340554.6:p.Thr22646=
ENST00000342992.10:c.86853A>T (TTN)	ENSP00000343764.6:p.Thr28951=
ENST00000359218.9:c.67737A>T (TTN)	ENSP00000352154.5:p.Thr22579=
ENST00000460472.6:c.67362A>T (TTN)	ENSP00000434586.1:p.Thr22454=
ENST00000589042.5:c.94557A>T (TTN) MANE Select	ENSP00000467141.1:p.Thr31519=
ENST00000591111.5:c.89634A>T (TTN)	ENSP00000465570.1:p.Thr29878=
ENST00000615779.4:c.89634A>T (TTN)	ENSP00000483597.1:p.Thr29878=
NM_001256850.1:c.89634A>T (TTN)	NP_001243779.1:p.Thr29878=
NM_001267550.2:c.94557A>T (TTN) MANE Select	NP_001254479.2:p.Thr31519=
NM_003319.4:c.67362A>T (TTN)	NP_003310.4:p.Thr22454=
NM_133378.4:c.86853A>T (TTN)	NP_596869.4:p.Thr28951=
NM_133432.3:c.67737A>T (TTN)	NP_597676.3:p.Thr22579=
NM_133437.4:c.67938A>T (TTN)	NP_597681.4:p.Thr22646=
NR_038271.1:n.446+23235T>A (TTN-AS1)
NR_038272.1:n.2043+4510T>A (TTN-AS1)
XM_011511729.1:c.93654A>T (TTN)	XP_011510031.1:p.Thr31218=
XM_011511730.1:c.67548A>T (TTN)	XP_011510032.1:p.Thr22516=
XM_011511731.1:c.67407A>T (TTN)	XP_011510033.1:p.Thr22469=
XM_017004819.1:c.93450A>T (TTN)	XP_016860308.1:p.Thr31150=
XM_017004820.1:c.88848A>T (TTN)	XP_016860309.1:p.Thr29616=
XM_017004821.1:c.88845A>T (TTN)	XP_016860310.1:p.Thr29615=
XM_017004822.1:c.85887A>T (TTN)	XP_016860311.1:p.Thr28629=
XM_017004823.1:c.67503A>T (TTN)	XP_016860312.1:p.Thr22501=
XM_024453094.1:c.88998A>T (TTN)	XP_024308862.1:p.Thr29666=
XM_024453095.1:c.88995A>T (TTN)	XP_024308863.1:p.Thr29665=
XM_024453096.1:c.88428A>T (TTN)	XP_024308864.1:p.Thr29476=
XM_024453097.1:c.85770A>T (TTN)	XP_024308865.1:p.Thr28590=
XM_024453098.1:c.85689A>T (TTN)	XP_024308866.1:p.Thr28563=
XM_024453099.1:c.67452A>T (TTN)	XP_024308867.1:p.Thr22484=
XM_024453100.1:c.57306A>T (TTN)	XP_024308868.1:p.Thr19102=