Canonical Allele Identifier: CA538437256

Gene: TTN

Linked Data

• gnomAD v2: 2-179554646-G-GTTGTGTTTAA
• MyVariant Identifiers: chr2:g.179554646_179554647insTTGTGTTTAA (hg19) ; chr2:g.178689919_178689920insTTGTGTTTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689921_178689922insGTGTTTAATT , CM000664.2:g.178689921_178689922insGTGTTTAATT	GRCh38
NC_000002.11:g.179554648_179554649insGTGTTTAATT , CM000664.1:g.179554648_179554649insGTGTTTAATT	GRCh37
NC_000002.10:g.179262893_179262894insGTGTTTAATT	NCBI36
NG_011618.3:g.145883_145884insTTAAACACAA , LRG_391:g.145883_145884insTTAAACACAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.28031-24_28031-23insTTAAACACAA	ENSP00000343764.6:n.28031-24_28031-23insT...
ENST00000342175.11:c.13859-47603_13859-47602insTTAAACACAA	ENSP00000340554.6:n.13859-47603_13859-476...
ENST00000359218.10:c.13658-47603_13658-47602insTTAAACACAA	ENSP00000352154.5:n.13658-47603_13658-476...
ENST00000342175.10:c.13859-47603_13859-47602insTTAAACACAA	ENSP00000340554.6:n.13859-47603_13859-476...
ENST00000342992.10:c.28031-24_28031-23insTTAAACACAA	ENSP00000343764.6:n.28031-24_28031-23insT...
ENST00000359218.9:c.13658-47603_13658-47602insTTAAACACAA	ENSP00000352154.5:n.13658-47603_13658-476...
ENST00000414766.5:c.1397-24_1397-23insTTAAACACAA	ENSP00000401501.1:n.1397-24_1397-23insTTA...
ENST00000460472.6:c.13283-47603_13283-47602insTTAAACACAA	ENSP00000434586.1:n.13283-47603_13283-476...
ENST00000589042.5:c.31763-24_31763-23insTTAAACACAA MANE Select	ENSP00000467141.1:n.31763-24_31763-23insT...
ENST00000591111.5:c.30812-24_30812-23insTTAAACACAA	ENSP00000465570.1:n.30812-24_30812-23insT...
ENST00000615779.4:c.30812-24_30812-23insTTAAACACAA	ENSP00000483597.1:n.30812-24_30812-23insT...
NM_001256850.1:c.30812-24_30812-23insTTAAACACAA	NP_001243779.1:n.30812-24_30812-23insTTAA...
NM_001267550.2:c.31763-24_31763-23insTTAAACACAA MANE Select	NP_001254479.2:n.31763-24_31763-23insTTAA...
NM_003319.4:c.13283-47603_13283-47602insTTAAACACAA	NP_003310.4:n.13283-47603_13283-47602insT...
NM_133378.4:c.28031-24_28031-23insTTAAACACAA	NP_596869.4:n.28031-24_28031-23insTTAAACA...
NM_133432.3:c.13658-47603_13658-47602insTTAAACACAA	NP_597676.3:n.13658-47603_13658-47602insT...
NM_133437.4:c.13859-47603_13859-47602insTTAAACACAA	NP_597681.4:n.13859-47603_13859-47602insT...
XM_011511729.1:c.30860-24_30860-23insTTAAACACAA	XP_011510031.1:n.30860-24_30860-23insTTAA...
XM_011511730.1:c.13469-47603_13469-47602insTTAAACACAA	XP_011510032.1:n.13469-47603_13469-47602i...
XM_011511731.1:c.13328-47603_13328-47602insTTAAACACAA	XP_011510033.1:n.13328-47603_13328-47602i...
XM_017004819.1:c.30815-24_30815-23insTTAAACACAA	XP_016860308.1:n.30815-24_30815-23insTTAA...
XM_017004820.1:c.28034-24_28034-23insTTAAACACAA	XP_016860309.1:n.28034-24_28034-23insTTAA...
XM_017004821.1:c.28031-24_28031-23insTTAAACACAA	XP_016860310.1:n.28031-24_28031-23insTTAA...
XM_017004822.1:c.30815-24_30815-23insTTAAACACAA	XP_016860311.1:n.30815-24_30815-23insTTAA...
XM_017004823.1:c.13424-47603_13424-47602insTTAAACACAA	XP_016860312.1:n.13424-47603_13424-47602i...
XM_024453094.1:c.30815-24_30815-23insTTAAACACAA	XP_024308862.1:n.30815-24_30815-23insTTAA...
XM_024453095.1:c.30815-24_30815-23insTTAAACACAA	XP_024308863.1:n.30815-24_30815-23insTTAA...
XM_024453096.1:c.30815-24_30815-23insTTAAACACAA	XP_024308864.1:n.30815-24_30815-23insTTAA...
XM_024453097.1:c.30815-24_30815-23insTTAAACACAA	XP_024308865.1:n.30815-24_30815-23insTTAA...
XM_024453098.1:c.30815-24_30815-23insTTAAACACAA	XP_024308866.1:n.30815-24_30815-23insTTAA...
XM_024453099.1:c.13424-47603_13424-47602insTTAAACACAA	XP_024308867.1:n.13424-47603_13424-47602i...