Canonical Allele Identifier: CA349522393

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178554217C>T , CM000664.2:g.178554217C>T	GRCh38
NC_000002.11:g.179418944C>T , CM000664.1:g.179418944C>T	GRCh37
NC_000002.10:g.179127190C>T	NCBI36
NG_011618.3:g.281586G>A , LRG_391:g.281586G>A
NG_051363.1:g.36391C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.88895-1G>A (TTN) MANE Select	NP_001254479.2:n.88895-1G>A
ENST00000589042.5:c.88895-1G>A (TTN) MANE Select	ENSP00000467141.1:n.88895-1G>A
NM_001256850.1:c.83972-1G>A (TTN)	NP_001243779.1:n.83972-1G>A
NM_003319.4:c.61700-1G>A (TTN)	NP_003310.4:n.61700-1G>A
NM_133378.4:c.81191-1G>A (TTN)	NP_596869.4:n.81191-1G>A
NM_133432.3:c.62075-1G>A (TTN)	NP_597676.3:n.62075-1G>A
NM_133437.4:c.62276-1G>A (TTN)	NP_597681.4:n.62276-1G>A
NR_038271.1:n.447-17083C>T (TTN-AS1)
NR_038272.1:n.2043+11856C>T (TTN-AS1)
ENST00000342175.10:c.62276-1G>A (TTN)	ENSP00000340554.6:n.62276-1G>A
ENST00000342175.11:c.62276-1G>A (TTN)	ENSP00000340554.6:n.62276-1G>A
ENST00000342992.10:c.81191-1G>A (TTN)	ENSP00000343764.6:n.81191-1G>A
ENST00000342992.11:c.81191-1G>A (TTN)	ENSP00000343764.6:n.81191-1G>A
ENST00000359218.10:c.62075-1G>A (TTN)	ENSP00000352154.5:n.62075-1G>A
ENST00000359218.9:c.62075-1G>A (TTN)	ENSP00000352154.5:n.62075-1G>A
ENST00000460472.6:c.61700-1G>A (TTN)	ENSP00000434586.1:n.61700-1G>A
ENST00000591111.5:c.83972-1G>A (TTN)	ENSP00000465570.1:n.83972-1G>A
ENST00000615779.4:c.83972-1G>A (TTN)	ENSP00000483597.1:n.83972-1G>A
XM_011511729.1:c.87992-1G>A (TTN)	XP_011510031.1:n.87992-1G>A
XM_011511730.1:c.61886-1G>A (TTN)	XP_011510032.1:n.61886-1G>A
XM_011511731.1:c.61745-1G>A (TTN)	XP_011510033.1:n.61745-1G>A
XM_017004819.1:c.87788-1G>A (TTN)	XP_016860308.1:n.87788-1G>A
XM_017004820.1:c.83186-1G>A (TTN)	XP_016860309.1:n.83186-1G>A
XM_017004821.1:c.83183-1G>A (TTN)	XP_016860310.1:n.83183-1G>A
XM_017004822.1:c.80225-1G>A (TTN)	XP_016860311.1:n.80225-1G>A
XM_017004823.1:c.61841-1G>A (TTN)	XP_016860312.1:n.61841-1G>A
XM_024453094.1:c.83336-1G>A (TTN)	XP_024308862.1:n.83336-1G>A
XM_024453095.1:c.83333-1G>A (TTN)	XP_024308863.1:n.83333-1G>A
XM_024453096.1:c.82766-1G>A (TTN)	XP_024308864.1:n.82766-1G>A
XM_024453097.1:c.80108-1G>A (TTN)	XP_024308865.1:n.80108-1G>A
XM_024453098.1:c.80027-1G>A (TTN)	XP_024308866.1:n.80027-1G>A
XM_024453099.1:c.61790-1G>A (TTN)	XP_024308867.1:n.61790-1G>A
XM_024453100.1:c.51644-1G>A (TTN)	XP_024308868.1:n.51644-1G>A