Canonical Allele Identifier: CA349441791

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178542565T>G , CM000664.2:g.178542565T>G	GRCh38
NC_000002.11:g.179407292T>G , CM000664.1:g.179407292T>G	GRCh37
NC_000002.10:g.179115538T>G	NCBI36
NG_011618.3:g.293238A>C , LRG_391:g.293238A>C
NG_051363.1:g.24739T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.97193-2A>C (TTN) MANE Select	NP_001254479.2:n.97193-2A>C
ENST00000589042.5:c.97193-2A>C (TTN) MANE Select	ENSP00000467141.1:n.97193-2A>C
NM_001256850.1:c.92270-2A>C (TTN)	NP_001243779.1:n.92270-2A>C
NM_003319.4:c.69998-2A>C (TTN)	NP_003310.4:n.69998-2A>C
NM_133378.4:c.89489-2A>C (TTN)	NP_596869.4:n.89489-2A>C
NM_133432.3:c.70373-2A>C (TTN)	NP_597676.3:n.70373-2A>C
NM_133437.4:c.70574-2A>C (TTN)	NP_597681.4:n.70574-2A>C
NR_038271.1:n.446+18929T>G (TTN-AS1)
NR_038272.1:n.2043+204T>G (TTN-AS1)
ENST00000342175.10:c.70574-2A>C (TTN)	ENSP00000340554.6:n.70574-2A>C
ENST00000342175.11:c.70574-2A>C (TTN)	ENSP00000340554.6:n.70574-2A>C
ENST00000342992.10:c.89489-2A>C (TTN)	ENSP00000343764.6:n.89489-2A>C
ENST00000342992.11:c.89489-2A>C (TTN)	ENSP00000343764.6:n.89489-2A>C
ENST00000359218.10:c.70373-2A>C (TTN)	ENSP00000352154.5:n.70373-2A>C
ENST00000359218.9:c.70373-2A>C (TTN)	ENSP00000352154.5:n.70373-2A>C
ENST00000460472.6:c.69998-2A>C (TTN)	ENSP00000434586.1:n.69998-2A>C
ENST00000591111.5:c.92270-2A>C (TTN)	ENSP00000465570.1:n.92270-2A>C
ENST00000615779.4:c.92270-2A>C (TTN)	ENSP00000483597.1:n.92270-2A>C
XM_011511729.1:c.96290-2A>C (TTN)	XP_011510031.1:n.96290-2A>C
XM_011511730.1:c.70184-2A>C (TTN)	XP_011510032.1:n.70184-2A>C
XM_011511731.1:c.70043-2A>C (TTN)	XP_011510033.1:n.70043-2A>C
XM_017004819.1:c.96086-2A>C (TTN)	XP_016860308.1:n.96086-2A>C
XM_017004820.1:c.91484-2A>C (TTN)	XP_016860309.1:n.91484-2A>C
XM_017004821.1:c.91481-2A>C (TTN)	XP_016860310.1:n.91481-2A>C
XM_017004822.1:c.88523-2A>C (TTN)	XP_016860311.1:n.88523-2A>C
XM_017004823.1:c.70139-2A>C (TTN)	XP_016860312.1:n.70139-2A>C
XM_024453094.1:c.91634-2A>C (TTN)	XP_024308862.1:n.91634-2A>C
XM_024453095.1:c.91631-2A>C (TTN)	XP_024308863.1:n.91631-2A>C
XM_024453096.1:c.91064-2A>C (TTN)	XP_024308864.1:n.91064-2A>C
XM_024453097.1:c.88406-2A>C (TTN)	XP_024308865.1:n.88406-2A>C
XM_024453098.1:c.88325-2A>C (TTN)	XP_024308866.1:n.88325-2A>C
XM_024453099.1:c.70088-2A>C (TTN)	XP_024308867.1:n.70088-2A>C
XM_024453100.1:c.59942-2A>C (TTN)	XP_024308868.1:n.59942-2A>C