Canonical Allele Identifier: CA349618186

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482782T>C (hg19) ; chr2:g.178618055T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618055T>C , CM000664.2:g.178618055T>C	GRCh38
NC_000002.11:g.179482782T>C , CM000664.1:g.179482782T>C	GRCh37
NC_000002.10:g.179191027T>C	NCBI36
NG_011618.3:g.217748A>G , LRG_391:g.217748A>G
NG_051363.1:g.100229T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.39592A>G (TTN)	ENSP00000343764.6:p.Thr13198Ala
ENST00000342175.11:c.20677A>G (TTN)	ENSP00000340554.6:p.Thr6893Ala
ENST00000359218.10:c.20476A>G (TTN)	ENSP00000352154.5:p.Thr6826Ala
ENST00000342175.10:c.20677A>G (TTN)	ENSP00000340554.6:p.Thr6893Ala
ENST00000342992.10:c.39592A>G (TTN)	ENSP00000343764.6:p.Thr13198Ala
ENST00000359218.9:c.20476A>G (TTN)	ENSP00000352154.5:p.Thr6826Ala
ENST00000460472.6:c.20101A>G (TTN)	ENSP00000434586.1:p.Thr6701Ala
ENST00000589042.5:c.47296A>G (TTN) MANE Select	ENSP00000467141.1:p.Thr15766Ala
ENST00000591111.5:c.42373A>G (TTN)	ENSP00000465570.1:p.Thr14125Ala
ENST00000615779.4:c.42373A>G (TTN)	ENSP00000483597.1:p.Thr14125Ala
NM_001256850.1:c.42373A>G (TTN)	NP_001243779.1:p.Thr14125Ala
NM_001267550.2:c.47296A>G (TTN) MANE Select	NP_001254479.2:p.Thr15766Ala
NM_003319.4:c.20101A>G (TTN)	NP_003310.4:p.Thr6701Ala
NM_133378.4:c.39592A>G (TTN)	NP_596869.4:p.Thr13198Ala
NM_133432.3:c.20476A>G (TTN)	NP_597676.3:p.Thr6826Ala
NM_133437.4:c.20677A>G (TTN)	NP_597681.4:p.Thr6893Ala
NR_038271.1:n.1605-1698T>C (TTN-AS1)
XM_011511729.1:c.46393A>G (TTN)	XP_011510031.1:p.Thr15465Ala
XM_011511730.1:c.20287A>G (TTN)	XP_011510032.1:p.Thr6763Ala
XM_011511731.1:c.20146A>G (TTN)	XP_011510033.1:p.Thr6716Ala
XM_017004819.1:c.46189A>G (TTN)	XP_016860308.1:p.Thr15397Ala
XM_017004820.1:c.41587A>G (TTN)	XP_016860309.1:p.Thr13863Ala
XM_017004821.1:c.41584A>G (TTN)	XP_016860310.1:p.Thr13862Ala
XM_017004822.1:c.38626A>G (TTN)	XP_016860311.1:p.Thr12876Ala
XM_017004823.1:c.20242A>G (TTN)	XP_016860312.1:p.Thr6748Ala
XM_024453094.1:c.41737A>G (TTN)	XP_024308862.1:p.Thr13913Ala
XM_024453095.1:c.41734A>G (TTN)	XP_024308863.1:p.Thr13912Ala
XM_024453096.1:c.41167A>G (TTN)	XP_024308864.1:p.Thr13723Ala
XM_024453097.1:c.38509A>G (TTN)	XP_024308865.1:p.Thr12837Ala
XM_024453098.1:c.38428A>G (TTN)	XP_024308866.1:p.Thr12810Ala
XM_024453099.1:c.20191A>G (TTN)	XP_024308867.1:p.Thr6731Ala
XM_024453100.1:c.10045A>G (TTN)	XP_024308868.1:p.Thr3349Ala