Canonical Allele Identifier: CA349405971

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394996G>C (hg19) ; chr2:g.178530269G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530269G>C , CM000664.2:g.178530269G>C	GRCh38
NC_000002.11:g.179394996G>C , CM000664.1:g.179394996G>C	GRCh37
NC_000002.10:g.179103242G>C	NCBI36
NG_011618.3:g.305534C>G , LRG_391:g.305534C>G
NG_051363.1:g.12443G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98642C>G (TTN)	ENSP00000343764.6:p.Pro32881Arg
ENST00000342175.11:c.79727C>G (TTN)	ENSP00000340554.6:p.Pro26576Arg
ENST00000359218.10:c.79526C>G (TTN)	ENSP00000352154.5:p.Pro26509Arg
ENST00000342175.10:c.79727C>G (TTN)	ENSP00000340554.6:p.Pro26576Arg
ENST00000342992.10:c.98642C>G (TTN)	ENSP00000343764.6:p.Pro32881Arg
ENST00000359218.9:c.79526C>G (TTN)	ENSP00000352154.5:p.Pro26509Arg
ENST00000460472.6:c.79151C>G (TTN)	ENSP00000434586.1:p.Pro26384Arg
ENST00000589042.5:c.106346C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro35449Arg
ENST00000591111.5:c.101423C>G (TTN)	ENSP00000465570.1:p.Pro33808Arg
ENST00000615779.4:c.101423C>G (TTN)	ENSP00000483597.1:p.Pro33808Arg
NM_001256850.1:c.101423C>G (TTN)	NP_001243779.1:p.Pro33808Arg
NM_001267550.2:c.106346C>G (TTN) MANE Select	NP_001254479.2:p.Pro35449Arg
NM_003319.4:c.79151C>G (TTN)	NP_003310.4:p.Pro26384Arg
NM_133378.4:c.98642C>G (TTN)	NP_596869.4:p.Pro32881Arg
NM_133432.3:c.79526C>G (TTN)	NP_597676.3:p.Pro26509Arg
NM_133437.4:c.79727C>G (TTN)	NP_597681.4:p.Pro26576Arg
NR_038271.1:n.446+6633G>C (TTN-AS1)
NR_038272.1:n.220-5463G>C (TTN-AS1)
XM_011511729.1:c.105443C>G (TTN)	XP_011510031.1:p.Pro35148Arg
XM_011511730.1:c.79337C>G (TTN)	XP_011510032.1:p.Pro26446Arg
XM_011511731.1:c.79196C>G (TTN)	XP_011510033.1:p.Pro26399Arg
XM_017004819.1:c.105239C>G (TTN)	XP_016860308.1:p.Pro35080Arg
XM_017004820.1:c.100637C>G (TTN)	XP_016860309.1:p.Pro33546Arg
XM_017004821.1:c.100634C>G (TTN)	XP_016860310.1:p.Pro33545Arg
XM_017004822.1:c.97676C>G (TTN)	XP_016860311.1:p.Pro32559Arg
XM_017004823.1:c.79292C>G (TTN)	XP_016860312.1:p.Pro26431Arg
XM_024453094.1:c.100787C>G (TTN)	XP_024308862.1:p.Pro33596Arg
XM_024453095.1:c.100784C>G (TTN)	XP_024308863.1:p.Pro33595Arg
XM_024453096.1:c.100217C>G (TTN)	XP_024308864.1:p.Pro33406Arg
XM_024453097.1:c.97559C>G (TTN)	XP_024308865.1:p.Pro32520Arg
XM_024453098.1:c.97478C>G (TTN)	XP_024308866.1:p.Pro32493Arg
XM_024453099.1:c.79241C>G (TTN)	XP_024308867.1:p.Pro26414Arg
XM_024453100.1:c.69095C>G (TTN)	XP_024308868.1:p.Pro23032Arg