Canonical Allele Identifier: CA1988816

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178561961T>C , CM000664.2:g.178561961T>C	GRCh38
NC_000002.11:g.179426688T>C , CM000664.1:g.179426688T>C	GRCh37
NC_000002.10:g.179134934T>C	NCBI36
NG_011618.3:g.273842A>G , LRG_391:g.273842A>G
NG_051363.1:g.44135T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.84171A>G (TTN) MANE Select	NP_001254479.2:p.Gly28057=
ENST00000589042.5:c.84171A>G (TTN) MANE Select	ENSP00000467141.1:p.Gly28057=
NM_001256850.1:c.79248A>G (TTN)	NP_001243779.1:p.Gly26416=
NM_003319.4:c.56976A>G (TTN)	NP_003310.4:p.Gly18992=
NM_133378.4:c.76467A>G (TTN)	NP_596869.4:p.Gly25489=
NM_133432.3:c.57351A>G (TTN)	NP_597676.3:p.Gly19117=
NM_133437.4:c.57552A>G (TTN)	NP_597681.4:p.Gly19184=
NR_038271.1:n.447-9339T>C (TTN-AS1)
NR_038272.1:n.2043+19600T>C (TTN-AS1)
ENST00000342175.10:c.57552A>G (TTN)	ENSP00000340554.6:p.Gly19184=
ENST00000342175.11:c.57552A>G (TTN)	ENSP00000340554.6:p.Gly19184=
ENST00000342992.10:c.76467A>G (TTN)	ENSP00000343764.6:p.Gly25489=
ENST00000342992.11:c.76467A>G (TTN)	ENSP00000343764.6:p.Gly25489=
ENST00000359218.10:c.57351A>G (TTN)	ENSP00000352154.5:p.Gly19117=
ENST00000359218.9:c.57351A>G (TTN)	ENSP00000352154.5:p.Gly19117=
ENST00000460472.6:c.56976A>G (TTN)	ENSP00000434586.1:p.Gly18992=
ENST00000591111.5:c.79248A>G (TTN)	ENSP00000465570.1:p.Gly26416=
ENST00000615779.4:c.79248A>G (TTN)	ENSP00000483597.1:p.Gly26416=
XM_011511729.1:c.83268A>G (TTN)	XP_011510031.1:p.Gly27756=
XM_011511730.1:c.57162A>G (TTN)	XP_011510032.1:p.Gly19054=
XM_011511731.1:c.57021A>G (TTN)	XP_011510033.1:p.Gly19007=
XM_017004819.1:c.83064A>G (TTN)	XP_016860308.1:p.Gly27688=
XM_017004820.1:c.78462A>G (TTN)	XP_016860309.1:p.Gly26154=
XM_017004821.1:c.78459A>G (TTN)	XP_016860310.1:p.Gly26153=
XM_017004822.1:c.75501A>G (TTN)	XP_016860311.1:p.Gly25167=
XM_017004823.1:c.57117A>G (TTN)	XP_016860312.1:p.Gly19039=
XM_024453094.1:c.78612A>G (TTN)	XP_024308862.1:p.Gly26204=
XM_024453095.1:c.78609A>G (TTN)	XP_024308863.1:p.Gly26203=
XM_024453096.1:c.78042A>G (TTN)	XP_024308864.1:p.Gly26014=
XM_024453097.1:c.75384A>G (TTN)	XP_024308865.1:p.Gly25128=
XM_024453098.1:c.75303A>G (TTN)	XP_024308866.1:p.Gly25101=
XM_024453099.1:c.57066A>G (TTN)	XP_024308867.1:p.Gly19022=
XM_024453100.1:c.46920A>G (TTN)	XP_024308868.1:p.Gly15640=