Canonical Allele Identifier: CA349436087

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179449407T>G (hg19) ; chr2:g.178584680T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584680T>G , CM000664.2:g.178584680T>G	GRCh38
NC_000002.11:g.179449407T>G , CM000664.1:g.179449407T>G	GRCh37
NC_000002.10:g.179157653T>G	NCBI36
NG_011618.3:g.251123A>C , LRG_391:g.251123A>C
NG_051363.1:g.66854T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57257A>C (TTN)	ENSP00000343764.6:p.Gln19086Pro
ENST00000342175.11:c.38342A>C (TTN)	ENSP00000340554.6:p.Gln12781Pro
ENST00000359218.10:c.38141A>C (TTN)	ENSP00000352154.5:p.Gln12714Pro
ENST00000342175.10:c.38342A>C (TTN)	ENSP00000340554.6:p.Gln12781Pro
ENST00000342992.10:c.57257A>C (TTN)	ENSP00000343764.6:p.Gln19086Pro
ENST00000359218.9:c.38141A>C (TTN)	ENSP00000352154.5:p.Gln12714Pro
ENST00000460472.6:c.37766A>C (TTN)	ENSP00000434586.1:p.Gln12589Pro
ENST00000589042.5:c.64961A>C (TTN) MANE Select	ENSP00000467141.1:p.Gln21654Pro
ENST00000591111.5:c.60038A>C (TTN)	ENSP00000465570.1:p.Gln20013Pro
ENST00000615779.4:c.60038A>C (TTN)	ENSP00000483597.1:p.Gln20013Pro
NM_001256850.1:c.60038A>C (TTN)	NP_001243779.1:p.Gln20013Pro
NM_001267550.2:c.64961A>C (TTN) MANE Select	NP_001254479.2:p.Gln21654Pro
NM_003319.4:c.37766A>C (TTN)	NP_003310.4:p.Gln12589Pro
NM_133378.4:c.57257A>C (TTN)	NP_596869.4:p.Gln19086Pro
NM_133432.3:c.38141A>C (TTN)	NP_597676.3:p.Gln12714Pro
NM_133437.4:c.38342A>C (TTN)	NP_597681.4:p.Gln12781Pro
NR_038271.1:n.597-12916T>G (TTN-AS1)
NR_038272.1:n.2875T>G (TTN-AS1)
XM_011511729.1:c.64058A>C (TTN)	XP_011510031.1:p.Gln21353Pro
XM_011511730.1:c.37952A>C (TTN)	XP_011510032.1:p.Gln12651Pro
XM_011511731.1:c.37811A>C (TTN)	XP_011510033.1:p.Gln12604Pro
XM_017004819.1:c.63854A>C (TTN)	XP_016860308.1:p.Gln21285Pro
XM_017004820.1:c.59252A>C (TTN)	XP_016860309.1:p.Gln19751Pro
XM_017004821.1:c.59249A>C (TTN)	XP_016860310.1:p.Gln19750Pro
XM_017004822.1:c.56291A>C (TTN)	XP_016860311.1:p.Gln18764Pro
XM_017004823.1:c.37907A>C (TTN)	XP_016860312.1:p.Gln12636Pro
XM_024453094.1:c.59402A>C (TTN)	XP_024308862.1:p.Gln19801Pro
XM_024453095.1:c.59399A>C (TTN)	XP_024308863.1:p.Gln19800Pro
XM_024453096.1:c.58832A>C (TTN)	XP_024308864.1:p.Gln19611Pro
XM_024453097.1:c.56174A>C (TTN)	XP_024308865.1:p.Gln18725Pro
XM_024453098.1:c.56093A>C (TTN)	XP_024308866.1:p.Gln18698Pro
XM_024453099.1:c.37856A>C (TTN)	XP_024308867.1:p.Gln12619Pro
XM_024453100.1:c.27710A>C (TTN)	XP_024308868.1:p.Gln9237Pro