Canonical Allele Identifier: CA349405580

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394828C>T (hg19) ; chr2:g.178530101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530101C>T , CM000664.2:g.178530101C>T	GRCh38
NC_000002.11:g.179394828C>T , CM000664.1:g.179394828C>T	GRCh37
NC_000002.10:g.179103074C>T	NCBI36
NG_011618.3:g.305702G>A , LRG_391:g.305702G>A
NG_051363.1:g.12275C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98686G>A (TTN)	ENSP00000343764.6:p.Gly32896Ser
ENST00000342175.11:c.79771G>A (TTN)	ENSP00000340554.6:p.Gly26591Ser
ENST00000359218.10:c.79570G>A (TTN)	ENSP00000352154.5:p.Gly26524Ser
ENST00000342175.10:c.79771G>A (TTN)	ENSP00000340554.6:p.Gly26591Ser
ENST00000342992.10:c.98686G>A (TTN)	ENSP00000343764.6:p.Gly32896Ser
ENST00000359218.9:c.79570G>A (TTN)	ENSP00000352154.5:p.Gly26524Ser
ENST00000460472.6:c.79195G>A (TTN)	ENSP00000434586.1:p.Gly26399Ser
ENST00000589042.5:c.106390G>A (TTN) MANE Select	ENSP00000467141.1:p.Gly35464Ser
ENST00000591111.5:c.101467G>A (TTN)	ENSP00000465570.1:p.Gly33823Ser
ENST00000615779.4:c.101467G>A (TTN)	ENSP00000483597.1:p.Gly33823Ser
NM_001256850.1:c.101467G>A (TTN)	NP_001243779.1:p.Gly33823Ser
NM_001267550.2:c.106390G>A (TTN) MANE Select	NP_001254479.2:p.Gly35464Ser
NM_003319.4:c.79195G>A (TTN)	NP_003310.4:p.Gly26399Ser
NM_133378.4:c.98686G>A (TTN)	NP_596869.4:p.Gly32896Ser
NM_133432.3:c.79570G>A (TTN)	NP_597676.3:p.Gly26524Ser
NM_133437.4:c.79771G>A (TTN)	NP_597681.4:p.Gly26591Ser
NR_038271.1:n.446+6465C>T (TTN-AS1)
NR_038272.1:n.220-5631C>T (TTN-AS1)
XM_011511729.1:c.105487G>A (TTN)	XP_011510031.1:p.Gly35163Ser
XM_011511730.1:c.79381G>A (TTN)	XP_011510032.1:p.Gly26461Ser
XM_011511731.1:c.79240G>A (TTN)	XP_011510033.1:p.Gly26414Ser
XM_017004819.1:c.105283G>A (TTN)	XP_016860308.1:p.Gly35095Ser
XM_017004820.1:c.100681G>A (TTN)	XP_016860309.1:p.Gly33561Ser
XM_017004821.1:c.100678G>A (TTN)	XP_016860310.1:p.Gly33560Ser
XM_017004822.1:c.97720G>A (TTN)	XP_016860311.1:p.Gly32574Ser
XM_017004823.1:c.79336G>A (TTN)	XP_016860312.1:p.Gly26446Ser
XM_024453094.1:c.100831G>A (TTN)	XP_024308862.1:p.Gly33611Ser
XM_024453095.1:c.100828G>A (TTN)	XP_024308863.1:p.Gly33610Ser
XM_024453096.1:c.100261G>A (TTN)	XP_024308864.1:p.Gly33421Ser
XM_024453097.1:c.97603G>A (TTN)	XP_024308865.1:p.Gly32535Ser
XM_024453098.1:c.97522G>A (TTN)	XP_024308866.1:p.Gly32508Ser
XM_024453099.1:c.79285G>A (TTN)	XP_024308867.1:p.Gly26429Ser
XM_024453100.1:c.69139G>A (TTN)	XP_024308868.1:p.Gly23047Ser