Canonical Allele Identifier: CA349620970

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179435178T>A (hg19) ; chr2:g.178570451T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570451T>A , CM000664.2:g.178570451T>A	GRCh38
NC_000002.11:g.179435178T>A , CM000664.1:g.179435178T>A	GRCh37
NC_000002.10:g.179143424T>A	NCBI36
NG_011618.3:g.265352A>T , LRG_391:g.265352A>T
NG_051363.1:g.52625T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.67977A>T (TTN)	ENSP00000343764.6:p.Lys22659Asn
ENST00000342175.11:c.49062A>T (TTN)	ENSP00000340554.6:p.Lys16354Asn
ENST00000359218.10:c.48861A>T (TTN)	ENSP00000352154.5:p.Lys16287Asn
ENST00000342175.10:c.49062A>T (TTN)	ENSP00000340554.6:p.Lys16354Asn
ENST00000342992.10:c.67977A>T (TTN)	ENSP00000343764.6:p.Lys22659Asn
ENST00000359218.9:c.48861A>T (TTN)	ENSP00000352154.5:p.Lys16287Asn
ENST00000460472.6:c.48486A>T (TTN)	ENSP00000434586.1:p.Lys16162Asn
ENST00000589042.5:c.75681A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys25227Asn
ENST00000591111.5:c.70758A>T (TTN)	ENSP00000465570.1:p.Lys23586Asn
ENST00000615779.4:c.70758A>T (TTN)	ENSP00000483597.1:p.Lys23586Asn
NM_001256850.1:c.70758A>T (TTN)	NP_001243779.1:p.Lys23586Asn
NM_001267550.2:c.75681A>T (TTN) MANE Select	NP_001254479.2:p.Lys25227Asn
NM_003319.4:c.48486A>T (TTN)	NP_003310.4:p.Lys16162Asn
NM_133378.4:c.67977A>T (TTN)	NP_596869.4:p.Lys22659Asn
NM_133432.3:c.48861A>T (TTN)	NP_597676.3:p.Lys16287Asn
NM_133437.4:c.49062A>T (TTN)	NP_597681.4:p.Lys16354Asn
NR_038271.1:n.447-849T>A (TTN-AS1)
NR_038272.1:n.2044-12121T>A (TTN-AS1)
XM_011511729.1:c.74778A>T (TTN)	XP_011510031.1:p.Lys24926Asn
XM_011511730.1:c.48672A>T (TTN)	XP_011510032.1:p.Lys16224Asn
XM_011511731.1:c.48531A>T (TTN)	XP_011510033.1:p.Lys16177Asn
XM_017004819.1:c.74574A>T (TTN)	XP_016860308.1:p.Lys24858Asn
XM_017004820.1:c.69972A>T (TTN)	XP_016860309.1:p.Lys23324Asn
XM_017004821.1:c.69969A>T (TTN)	XP_016860310.1:p.Lys23323Asn
XM_017004822.1:c.67011A>T (TTN)	XP_016860311.1:p.Lys22337Asn
XM_017004823.1:c.48627A>T (TTN)	XP_016860312.1:p.Lys16209Asn
XM_024453094.1:c.70122A>T (TTN)	XP_024308862.1:p.Lys23374Asn
XM_024453095.1:c.70119A>T (TTN)	XP_024308863.1:p.Lys23373Asn
XM_024453096.1:c.69552A>T (TTN)	XP_024308864.1:p.Lys23184Asn
XM_024453097.1:c.66894A>T (TTN)	XP_024308865.1:p.Lys22298Asn
XM_024453098.1:c.66813A>T (TTN)	XP_024308866.1:p.Lys22271Asn
XM_024453099.1:c.48576A>T (TTN)	XP_024308867.1:p.Lys16192Asn
XM_024453100.1:c.38430A>T (TTN)	XP_024308868.1:p.Lys12810Asn