Canonical Allele Identifier: CA349406886

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395188T>C (hg19) ; chr2:g.178530461T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530461T>C , CM000664.2:g.178530461T>C	GRCh38
NC_000002.11:g.179395188T>C , CM000664.1:g.179395188T>C	GRCh37
NC_000002.10:g.179103434T>C	NCBI36
NG_011618.3:g.305342A>G , LRG_391:g.305342A>G
NG_051363.1:g.12635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98450A>G (TTN)	ENSP00000343764.6:p.Lys32817Arg
ENST00000342175.11:c.79535A>G (TTN)	ENSP00000340554.6:p.Lys26512Arg
ENST00000359218.10:c.79334A>G (TTN)	ENSP00000352154.5:p.Lys26445Arg
ENST00000342175.10:c.79535A>G (TTN)	ENSP00000340554.6:p.Lys26512Arg
ENST00000342992.10:c.98450A>G (TTN)	ENSP00000343764.6:p.Lys32817Arg
ENST00000359218.9:c.79334A>G (TTN)	ENSP00000352154.5:p.Lys26445Arg
ENST00000460472.6:c.78959A>G (TTN)	ENSP00000434586.1:p.Lys26320Arg
ENST00000589042.5:c.106154A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35385Arg
ENST00000591111.5:c.101231A>G (TTN)	ENSP00000465570.1:p.Lys33744Arg
ENST00000615779.4:c.101231A>G (TTN)	ENSP00000483597.1:p.Lys33744Arg
NM_001256850.1:c.101231A>G (TTN)	NP_001243779.1:p.Lys33744Arg
NM_001267550.2:c.106154A>G (TTN) MANE Select	NP_001254479.2:p.Lys35385Arg
NM_003319.4:c.78959A>G (TTN)	NP_003310.4:p.Lys26320Arg
NM_133378.4:c.98450A>G (TTN)	NP_596869.4:p.Lys32817Arg
NM_133432.3:c.79334A>G (TTN)	NP_597676.3:p.Lys26445Arg
NM_133437.4:c.79535A>G (TTN)	NP_597681.4:p.Lys26512Arg
NR_038271.1:n.446+6825T>C (TTN-AS1)
NR_038272.1:n.220-5271T>C (TTN-AS1)
XM_011511729.1:c.105251A>G (TTN)	XP_011510031.1:p.Lys35084Arg
XM_011511730.1:c.79145A>G (TTN)	XP_011510032.1:p.Lys26382Arg
XM_011511731.1:c.79004A>G (TTN)	XP_011510033.1:p.Lys26335Arg
XM_017004819.1:c.105047A>G (TTN)	XP_016860308.1:p.Lys35016Arg
XM_017004820.1:c.100445A>G (TTN)	XP_016860309.1:p.Lys33482Arg
XM_017004821.1:c.100442A>G (TTN)	XP_016860310.1:p.Lys33481Arg
XM_017004822.1:c.97484A>G (TTN)	XP_016860311.1:p.Lys32495Arg
XM_017004823.1:c.79100A>G (TTN)	XP_016860312.1:p.Lys26367Arg
XM_024453094.1:c.100595A>G (TTN)	XP_024308862.1:p.Lys33532Arg
XM_024453095.1:c.100592A>G (TTN)	XP_024308863.1:p.Lys33531Arg
XM_024453096.1:c.100025A>G (TTN)	XP_024308864.1:p.Lys33342Arg
XM_024453097.1:c.97367A>G (TTN)	XP_024308865.1:p.Lys32456Arg
XM_024453098.1:c.97286A>G (TTN)	XP_024308866.1:p.Lys32429Arg
XM_024453099.1:c.79049A>G (TTN)	XP_024308867.1:p.Lys26350Arg
XM_024453100.1:c.68903A>G (TTN)	XP_024308868.1:p.Lys22968Arg