Canonical Allele Identifier: CA349562711

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178605714C>T , CM000664.2:g.178605714C>T	GRCh38
NC_000002.11:g.179470441C>T , CM000664.1:g.179470441C>T	GRCh37
NC_000002.10:g.179178686C>T	NCBI36
NG_011618.3:g.230089G>A , LRG_391:g.230089G>A
NG_051363.1:g.87888C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.53582-1G>A (TTN) MANE Select	NP_001254479.2:n.53582-1G>A
ENST00000589042.5:c.53582-1G>A (TTN) MANE Select	ENSP00000467141.1:n.53582-1G>A
NM_001256850.1:c.48659-1G>A (TTN)	NP_001243779.1:n.48659-1G>A
NM_003319.4:c.26387-1G>A (TTN)	NP_003310.4:n.26387-1G>A
NM_133378.4:c.45878-1G>A (TTN)	NP_596869.4:n.45878-1G>A
NM_133432.3:c.26762-1G>A (TTN)	NP_597676.3:n.26762-1G>A
NM_133437.4:c.26963-1G>A (TTN)	NP_597681.4:n.26963-1G>A
NR_038271.1:n.683-2453C>T (TTN-AS1)
ENST00000342175.10:c.26963-1G>A (TTN)	ENSP00000340554.6:n.26963-1G>A
ENST00000342175.11:c.26963-1G>A (TTN)	ENSP00000340554.6:n.26963-1G>A
ENST00000342992.10:c.45878-1G>A (TTN)	ENSP00000343764.6:n.45878-1G>A
ENST00000342992.11:c.45878-1G>A (TTN)	ENSP00000343764.6:n.45878-1G>A
ENST00000359218.10:c.26762-1G>A (TTN)	ENSP00000352154.5:n.26762-1G>A
ENST00000359218.9:c.26762-1G>A (TTN)	ENSP00000352154.5:n.26762-1G>A
ENST00000460472.6:c.26387-1G>A (TTN)	ENSP00000434586.1:n.26387-1G>A
ENST00000591111.5:c.48659-1G>A (TTN)	ENSP00000465570.1:n.48659-1G>A
ENST00000615779.4:c.48659-1G>A (TTN)	ENSP00000483597.1:n.48659-1G>A
XM_011511729.1:c.52679-1G>A (TTN)	XP_011510031.1:n.52679-1G>A
XM_011511730.1:c.26573-1G>A (TTN)	XP_011510032.1:n.26573-1G>A
XM_011511731.1:c.26432-1G>A (TTN)	XP_011510033.1:n.26432-1G>A
XM_017004819.1:c.52475-1G>A (TTN)	XP_016860308.1:n.52475-1G>A
XM_017004820.1:c.47873-1G>A (TTN)	XP_016860309.1:n.47873-1G>A
XM_017004821.1:c.47870-1G>A (TTN)	XP_016860310.1:n.47870-1G>A
XM_017004822.1:c.44912-1G>A (TTN)	XP_016860311.1:n.44912-1G>A
XM_017004823.1:c.26528-1G>A (TTN)	XP_016860312.1:n.26528-1G>A
XM_024453094.1:c.48023-1G>A (TTN)	XP_024308862.1:n.48023-1G>A
XM_024453095.1:c.48020-1G>A (TTN)	XP_024308863.1:n.48020-1G>A
XM_024453096.1:c.47453-1G>A (TTN)	XP_024308864.1:n.47453-1G>A
XM_024453097.1:c.44795-1G>A (TTN)	XP_024308865.1:n.44795-1G>A
XM_024453098.1:c.44714-1G>A (TTN)	XP_024308866.1:n.44714-1G>A
XM_024453099.1:c.26477-1G>A (TTN)	XP_024308867.1:n.26477-1G>A
XM_024453100.1:c.16331-1G>A (TTN)	XP_024308868.1:n.16331-1G>A