Canonical Allele Identifier: CA349673338

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178578716C>T , CM000664.2:g.178578716C>T	GRCh38
NC_000002.11:g.179443443C>T , CM000664.1:g.179443443C>T	GRCh37
NC_000002.10:g.179151689C>T	NCBI36
NG_011618.3:g.257087G>A , LRG_391:g.257087G>A
NG_051363.1:g.60890C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.68225-1G>A (TTN) MANE Select	NP_001254479.2:n.68225-1G>A
ENST00000589042.5:c.68225-1G>A (TTN) MANE Select	ENSP00000467141.1:n.68225-1G>A
NM_001256850.1:c.63302-1G>A (TTN)	NP_001243779.1:n.63302-1G>A
NM_003319.4:c.41030-1G>A (TTN)	NP_003310.4:n.41030-1G>A
NM_133378.4:c.60521-1G>A (TTN)	NP_596869.4:n.60521-1G>A
NM_133432.3:c.41405-1G>A (TTN)	NP_597676.3:n.41405-1G>A
NM_133437.4:c.41606-1G>A (TTN)	NP_597681.4:n.41606-1G>A
NR_038271.1:n.596+7267C>T (TTN-AS1)
NR_038272.1:n.2044-3856C>T (TTN-AS1)
ENST00000342175.10:c.41606-1G>A (TTN)	ENSP00000340554.6:n.41606-1G>A
ENST00000342175.11:c.41606-1G>A (TTN)	ENSP00000340554.6:n.41606-1G>A
ENST00000342992.10:c.60521-1G>A (TTN)	ENSP00000343764.6:n.60521-1G>A
ENST00000342992.11:c.60521-1G>A (TTN)	ENSP00000343764.6:n.60521-1G>A
ENST00000359218.10:c.41405-1G>A (TTN)	ENSP00000352154.5:n.41405-1G>A
ENST00000359218.9:c.41405-1G>A (TTN)	ENSP00000352154.5:n.41405-1G>A
ENST00000460472.6:c.41030-1G>A (TTN)	ENSP00000434586.1:n.41030-1G>A
ENST00000591111.5:c.63302-1G>A (TTN)	ENSP00000465570.1:n.63302-1G>A
ENST00000615779.4:c.63302-1G>A (TTN)	ENSP00000483597.1:n.63302-1G>A
XM_011511729.1:c.67322-1G>A (TTN)	XP_011510031.1:n.67322-1G>A
XM_011511730.1:c.41216-1G>A (TTN)	XP_011510032.1:n.41216-1G>A
XM_011511731.1:c.41075-1G>A (TTN)	XP_011510033.1:n.41075-1G>A
XM_017004819.1:c.67118-1G>A (TTN)	XP_016860308.1:n.67118-1G>A
XM_017004820.1:c.62516-1G>A (TTN)	XP_016860309.1:n.62516-1G>A
XM_017004821.1:c.62513-1G>A (TTN)	XP_016860310.1:n.62513-1G>A
XM_017004822.1:c.59555-1G>A (TTN)	XP_016860311.1:n.59555-1G>A
XM_017004823.1:c.41171-1G>A (TTN)	XP_016860312.1:n.41171-1G>A
XM_024453094.1:c.62666-1G>A (TTN)	XP_024308862.1:n.62666-1G>A
XM_024453095.1:c.62663-1G>A (TTN)	XP_024308863.1:n.62663-1G>A
XM_024453096.1:c.62096-1G>A (TTN)	XP_024308864.1:n.62096-1G>A
XM_024453097.1:c.59438-1G>A (TTN)	XP_024308865.1:n.59438-1G>A
XM_024453098.1:c.59357-1G>A (TTN)	XP_024308866.1:n.59357-1G>A
XM_024453099.1:c.41120-1G>A (TTN)	XP_024308867.1:n.41120-1G>A
XM_024453100.1:c.30974-1G>A (TTN)	XP_024308868.1:n.30974-1G>A