Canonical Allele Identifier: CA349435482

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179449212C>A (hg19) ; chr2:g.178584485C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584485C>A , CM000664.2:g.178584485C>A	GRCh38
NC_000002.11:g.179449212C>A , CM000664.1:g.179449212C>A	GRCh37
NC_000002.10:g.179157458C>A	NCBI36
NG_011618.3:g.251318G>T , LRG_391:g.251318G>T
NG_051363.1:g.66659C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57362G>T (TTN)	ENSP00000343764.6:p.Ser19121Ile
ENST00000342175.11:c.38447G>T (TTN)	ENSP00000340554.6:p.Ser12816Ile
ENST00000359218.10:c.38246G>T (TTN)	ENSP00000352154.5:p.Ser12749Ile
ENST00000342175.10:c.38447G>T (TTN)	ENSP00000340554.6:p.Ser12816Ile
ENST00000342992.10:c.57362G>T (TTN)	ENSP00000343764.6:p.Ser19121Ile
ENST00000359218.9:c.38246G>T (TTN)	ENSP00000352154.5:p.Ser12749Ile
ENST00000460472.6:c.37871G>T (TTN)	ENSP00000434586.1:p.Ser12624Ile
ENST00000589042.5:c.65066G>T (TTN) MANE Select	ENSP00000467141.1:p.Ser21689Ile
ENST00000591111.5:c.60143G>T (TTN)	ENSP00000465570.1:p.Ser20048Ile
ENST00000615779.4:c.60143G>T (TTN)	ENSP00000483597.1:p.Ser20048Ile
NM_001256850.1:c.60143G>T (TTN)	NP_001243779.1:p.Ser20048Ile
NM_001267550.2:c.65066G>T (TTN) MANE Select	NP_001254479.2:p.Ser21689Ile
NM_003319.4:c.37871G>T (TTN)	NP_003310.4:p.Ser12624Ile
NM_133378.4:c.57362G>T (TTN)	NP_596869.4:p.Ser19121Ile
NM_133432.3:c.38246G>T (TTN)	NP_597676.3:p.Ser12749Ile
NM_133437.4:c.38447G>T (TTN)	NP_597681.4:p.Ser12816Ile
NR_038271.1:n.596+13036C>A (TTN-AS1)
NR_038272.1:n.2768-88C>A (TTN-AS1)
XM_011511729.1:c.64163G>T (TTN)	XP_011510031.1:p.Ser21388Ile
XM_011511730.1:c.38057G>T (TTN)	XP_011510032.1:p.Ser12686Ile
XM_011511731.1:c.37916G>T (TTN)	XP_011510033.1:p.Ser12639Ile
XM_017004819.1:c.63959G>T (TTN)	XP_016860308.1:p.Ser21320Ile
XM_017004820.1:c.59357G>T (TTN)	XP_016860309.1:p.Ser19786Ile
XM_017004821.1:c.59354G>T (TTN)	XP_016860310.1:p.Ser19785Ile
XM_017004822.1:c.56396G>T (TTN)	XP_016860311.1:p.Ser18799Ile
XM_017004823.1:c.38012G>T (TTN)	XP_016860312.1:p.Ser12671Ile
XM_024453094.1:c.59507G>T (TTN)	XP_024308862.1:p.Ser19836Ile
XM_024453095.1:c.59504G>T (TTN)	XP_024308863.1:p.Ser19835Ile
XM_024453096.1:c.58937G>T (TTN)	XP_024308864.1:p.Ser19646Ile
XM_024453097.1:c.56279G>T (TTN)	XP_024308865.1:p.Ser18760Ile
XM_024453098.1:c.56198G>T (TTN)	XP_024308866.1:p.Ser18733Ile
XM_024453099.1:c.37961G>T (TTN)	XP_024308867.1:p.Ser12654Ile
XM_024453100.1:c.27815G>T (TTN)	XP_024308868.1:p.Ser9272Ile