Canonical Allele Identifier: CA1986328

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539260A>G , CM000664.2:g.178539260A>G	GRCh38
NC_000002.11:g.179403987A>G , CM000664.1:g.179403987A>G	GRCh37
NC_000002.10:g.179112233A>G	NCBI36
NG_011618.3:g.296543T>C , LRG_391:g.296543T>C
NG_051363.1:g.21434A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.98684-9T>C (TTN) MANE Select	NP_001254479.2:n.98684-9T>C
ENST00000589042.5:c.98684-9T>C (TTN) MANE Select	ENSP00000467141.1:n.98684-9T>C
NM_001256850.1:c.93761-9T>C (TTN)	NP_001243779.1:n.93761-9T>C
NM_003319.4:c.71489-9T>C (TTN)	NP_003310.4:n.71489-9T>C
NM_133378.4:c.90980-9T>C (TTN)	NP_596869.4:n.90980-9T>C
NM_133432.3:c.71864-9T>C (TTN)	NP_597676.3:n.71864-9T>C
NM_133437.4:c.72065-9T>C (TTN)	NP_597681.4:n.72065-9T>C
NR_038271.1:n.446+15624A>G (TTN-AS1)
NR_038272.1:n.1210A>G (TTN-AS1)
ENST00000342175.10:c.72065-9T>C (TTN)	ENSP00000340554.6:n.72065-9T>C
ENST00000342175.11:c.72065-9T>C (TTN)	ENSP00000340554.6:n.72065-9T>C
ENST00000342992.10:c.90980-9T>C (TTN)	ENSP00000343764.6:n.90980-9T>C
ENST00000342992.11:c.90980-9T>C (TTN)	ENSP00000343764.6:n.90980-9T>C
ENST00000359218.10:c.71864-9T>C (TTN)	ENSP00000352154.5:n.71864-9T>C
ENST00000359218.9:c.71864-9T>C (TTN)	ENSP00000352154.5:n.71864-9T>C
ENST00000460472.6:c.71489-9T>C (TTN)	ENSP00000434586.1:n.71489-9T>C
ENST00000591111.5:c.93761-9T>C (TTN)	ENSP00000465570.1:n.93761-9T>C
ENST00000615779.4:c.93761-9T>C (TTN)	ENSP00000483597.1:n.93761-9T>C
XM_011511729.1:c.97781-9T>C (TTN)	XP_011510031.1:n.97781-9T>C
XM_011511730.1:c.71675-9T>C (TTN)	XP_011510032.1:n.71675-9T>C
XM_011511731.1:c.71534-9T>C (TTN)	XP_011510033.1:n.71534-9T>C
XM_017004819.1:c.97577-9T>C (TTN)	XP_016860308.1:n.97577-9T>C
XM_017004820.1:c.92975-9T>C (TTN)	XP_016860309.1:n.92975-9T>C
XM_017004821.1:c.92972-9T>C (TTN)	XP_016860310.1:n.92972-9T>C
XM_017004822.1:c.90014-9T>C (TTN)	XP_016860311.1:n.90014-9T>C
XM_017004823.1:c.71630-9T>C (TTN)	XP_016860312.1:n.71630-9T>C
XM_024453094.1:c.93125-9T>C (TTN)	XP_024308862.1:n.93125-9T>C
XM_024453095.1:c.93122-9T>C (TTN)	XP_024308863.1:n.93122-9T>C
XM_024453096.1:c.92555-9T>C (TTN)	XP_024308864.1:n.92555-9T>C
XM_024453097.1:c.89897-9T>C (TTN)	XP_024308865.1:n.89897-9T>C
XM_024453098.1:c.89816-9T>C (TTN)	XP_024308866.1:n.89816-9T>C
XM_024453099.1:c.71579-9T>C (TTN)	XP_024308867.1:n.71579-9T>C
XM_024453100.1:c.61433-9T>C (TTN)	XP_024308868.1:n.61433-9T>C