Canonical Allele Identifier: CA430094059

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394826A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530099A>T , CM000664.2:g.178530099A>T	GRCh38
NC_000002.11:g.179394826A>T , CM000664.1:g.179394826A>T	GRCh37
NC_000002.10:g.179103072A>T	NCBI36
NG_011618.3:g.305704T>A , LRG_391:g.305704T>A
NG_051363.1:g.12273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98688T>A (TTN)	ENSP00000343764.6:p.Gly32896=
ENST00000342175.11:c.79773T>A (TTN)	ENSP00000340554.6:p.Gly26591=
ENST00000359218.10:c.79572T>A (TTN)	ENSP00000352154.5:p.Gly26524=
ENST00000342175.10:c.79773T>A (TTN)	ENSP00000340554.6:p.Gly26591=
ENST00000342992.10:c.98688T>A (TTN)	ENSP00000343764.6:p.Gly32896=
ENST00000359218.9:c.79572T>A (TTN)	ENSP00000352154.5:p.Gly26524=
ENST00000460472.6:c.79197T>A (TTN)	ENSP00000434586.1:p.Gly26399=
ENST00000589042.5:c.106392T>A (TTN) MANE Select	ENSP00000467141.1:p.Gly35464=
ENST00000591111.5:c.101469T>A (TTN)	ENSP00000465570.1:p.Gly33823=
ENST00000615779.4:c.101469T>A (TTN)	ENSP00000483597.1:p.Gly33823=
NM_001256850.1:c.101469T>A (TTN)	NP_001243779.1:p.Gly33823=
NM_001267550.2:c.106392T>A (TTN) MANE Select	NP_001254479.2:p.Gly35464=
NM_003319.4:c.79197T>A (TTN)	NP_003310.4:p.Gly26399=
NM_133378.4:c.98688T>A (TTN)	NP_596869.4:p.Gly32896=
NM_133432.3:c.79572T>A (TTN)	NP_597676.3:p.Gly26524=
NM_133437.4:c.79773T>A (TTN)	NP_597681.4:p.Gly26591=
NR_038271.1:n.446+6463A>T (TTN-AS1)
NR_038272.1:n.220-5633A>T (TTN-AS1)
XM_011511729.1:c.105489T>A (TTN)	XP_011510031.1:p.Gly35163=
XM_011511730.1:c.79383T>A (TTN)	XP_011510032.1:p.Gly26461=
XM_011511731.1:c.79242T>A (TTN)	XP_011510033.1:p.Gly26414=
XM_017004819.1:c.105285T>A (TTN)	XP_016860308.1:p.Gly35095=
XM_017004820.1:c.100683T>A (TTN)	XP_016860309.1:p.Gly33561=
XM_017004821.1:c.100680T>A (TTN)	XP_016860310.1:p.Gly33560=
XM_017004822.1:c.97722T>A (TTN)	XP_016860311.1:p.Gly32574=
XM_017004823.1:c.79338T>A (TTN)	XP_016860312.1:p.Gly26446=
XM_024453094.1:c.100833T>A (TTN)	XP_024308862.1:p.Gly33611=
XM_024453095.1:c.100830T>A (TTN)	XP_024308863.1:p.Gly33610=
XM_024453096.1:c.100263T>A (TTN)	XP_024308864.1:p.Gly33421=
XM_024453097.1:c.97605T>A (TTN)	XP_024308865.1:p.Gly32535=
XM_024453098.1:c.97524T>A (TTN)	XP_024308866.1:p.Gly32508=
XM_024453099.1:c.79287T>A (TTN)	XP_024308867.1:p.Gly26429=
XM_024453100.1:c.69141T>A (TTN)	XP_024308868.1:p.Gly23047=