Canonical Allele Identifier: CA349488461

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179456608G>A (hg19) ; chr2:g.178591881G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591881G>A , CM000664.2:g.178591881G>A	GRCh38
NC_000002.11:g.179456608G>A , CM000664.1:g.179456608G>A	GRCh37
NC_000002.10:g.179164854G>A	NCBI36
NG_011618.3:g.243922C>T , LRG_391:g.243922C>T
NG_051363.1:g.74055G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52234C>T (TTN)	ENSP00000343764.6:p.Pro17412Ser
ENST00000342175.11:c.33319C>T (TTN)	ENSP00000340554.6:p.Pro11107Ser
ENST00000359218.10:c.33118C>T (TTN)	ENSP00000352154.5:p.Pro11040Ser
ENST00000342175.10:c.33319C>T (TTN)	ENSP00000340554.6:p.Pro11107Ser
ENST00000342992.10:c.52234C>T (TTN)	ENSP00000343764.6:p.Pro17412Ser
ENST00000359218.9:c.33118C>T (TTN)	ENSP00000352154.5:p.Pro11040Ser
ENST00000460472.6:c.32743C>T (TTN)	ENSP00000434586.1:p.Pro10915Ser
ENST00000589042.5:c.59938C>T (TTN) MANE Select	ENSP00000467141.1:p.Pro19980Ser
ENST00000591111.5:c.55015C>T (TTN)	ENSP00000465570.1:p.Pro18339Ser
ENST00000615779.4:c.55015C>T (TTN)	ENSP00000483597.1:p.Pro18339Ser
NM_001256850.1:c.55015C>T (TTN)	NP_001243779.1:p.Pro18339Ser
NM_001267550.2:c.59938C>T (TTN) MANE Select	NP_001254479.2:p.Pro19980Ser
NM_003319.4:c.32743C>T (TTN)	NP_003310.4:p.Pro10915Ser
NM_133378.4:c.52234C>T (TTN)	NP_596869.4:p.Pro17412Ser
NM_133432.3:c.33118C>T (TTN)	NP_597676.3:p.Pro11040Ser
NM_133437.4:c.33319C>T (TTN)	NP_597681.4:p.Pro11107Ser
NR_038271.1:n.597-5715G>A (TTN-AS1)
NR_038272.1:n.3364+567G>A (TTN-AS1)
XM_011511729.1:c.59035C>T (TTN)	XP_011510031.1:p.Pro19679Ser
XM_011511730.1:c.32929C>T (TTN)	XP_011510032.1:p.Pro10977Ser
XM_011511731.1:c.32788C>T (TTN)	XP_011510033.1:p.Pro10930Ser
XM_017004819.1:c.58831C>T (TTN)	XP_016860308.1:p.Pro19611Ser
XM_017004820.1:c.54229C>T (TTN)	XP_016860309.1:p.Pro18077Ser
XM_017004821.1:c.54226C>T (TTN)	XP_016860310.1:p.Pro18076Ser
XM_017004822.1:c.51268C>T (TTN)	XP_016860311.1:p.Pro17090Ser
XM_017004823.1:c.32884C>T (TTN)	XP_016860312.1:p.Pro10962Ser
XM_024453094.1:c.54379C>T (TTN)	XP_024308862.1:p.Pro18127Ser
XM_024453095.1:c.54376C>T (TTN)	XP_024308863.1:p.Pro18126Ser
XM_024453096.1:c.53809C>T (TTN)	XP_024308864.1:p.Pro17937Ser
XM_024453097.1:c.51151C>T (TTN)	XP_024308865.1:p.Pro17051Ser
XM_024453098.1:c.51070C>T (TTN)	XP_024308866.1:p.Pro17024Ser
XM_024453099.1:c.32833C>T (TTN)	XP_024308867.1:p.Pro10945Ser
XM_024453100.1:c.22687C>T (TTN)	XP_024308868.1:p.Pro7563Ser