Canonical Allele Identifier: CA349666227

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178576294G>A , CM000664.2:g.178576294G>A	GRCh38
NC_000002.11:g.179441021G>A , CM000664.1:g.179441021G>A	GRCh37
NC_000002.10:g.179149267G>A	NCBI36
NG_011618.3:g.259509C>T , LRG_391:g.259509C>T
NG_051363.1:g.58468G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.69838C>T (TTN) MANE Select	NP_001254479.2:p.Gln23280Ter
ENST00000589042.5:c.69838C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln23280Ter
NM_001256850.1:c.64915C>T (TTN)	NP_001243779.1:p.Gln21639Ter
NM_003319.4:c.42643C>T (TTN)	NP_003310.4:p.Gln14215Ter
NM_133378.4:c.62134C>T (TTN)	NP_596869.4:p.Gln20712Ter
NM_133432.3:c.43018C>T (TTN)	NP_597676.3:p.Gln14340Ter
NM_133437.4:c.43219C>T (TTN)	NP_597681.4:p.Gln14407Ter
NR_038271.1:n.596+4845G>A (TTN-AS1)
NR_038272.1:n.2044-6278G>A (TTN-AS1)
ENST00000342175.10:c.43219C>T (TTN)	ENSP00000340554.6:p.Gln14407Ter
ENST00000342175.11:c.43219C>T (TTN)	ENSP00000340554.6:p.Gln14407Ter
ENST00000342992.10:c.62134C>T (TTN)	ENSP00000343764.6:p.Gln20712Ter
ENST00000342992.11:c.62134C>T (TTN)	ENSP00000343764.6:p.Gln20712Ter
ENST00000359218.10:c.43018C>T (TTN)	ENSP00000352154.5:p.Gln14340Ter
ENST00000359218.9:c.43018C>T (TTN)	ENSP00000352154.5:p.Gln14340Ter
ENST00000460472.6:c.42643C>T (TTN)	ENSP00000434586.1:p.Gln14215Ter
ENST00000591111.5:c.64915C>T (TTN)	ENSP00000465570.1:p.Gln21639Ter
ENST00000615779.4:c.64915C>T (TTN)	ENSP00000483597.1:p.Gln21639Ter
XM_011511729.1:c.68935C>T (TTN)	XP_011510031.1:p.Gln22979Ter
XM_011511730.1:c.42829C>T (TTN)	XP_011510032.1:p.Gln14277Ter
XM_011511731.1:c.42688C>T (TTN)	XP_011510033.1:p.Gln14230Ter
XM_017004819.1:c.68731C>T (TTN)	XP_016860308.1:p.Gln22911Ter
XM_017004820.1:c.64129C>T (TTN)	XP_016860309.1:p.Gln21377Ter
XM_017004821.1:c.64126C>T (TTN)	XP_016860310.1:p.Gln21376Ter
XM_017004822.1:c.61168C>T (TTN)	XP_016860311.1:p.Gln20390Ter
XM_017004823.1:c.42784C>T (TTN)	XP_016860312.1:p.Gln14262Ter
XM_024453094.1:c.64279C>T (TTN)	XP_024308862.1:p.Gln21427Ter
XM_024453095.1:c.64276C>T (TTN)	XP_024308863.1:p.Gln21426Ter
XM_024453096.1:c.63709C>T (TTN)	XP_024308864.1:p.Gln21237Ter
XM_024453097.1:c.61051C>T (TTN)	XP_024308865.1:p.Gln20351Ter
XM_024453098.1:c.60970C>T (TTN)	XP_024308866.1:p.Gln20324Ter
XM_024453099.1:c.42733C>T (TTN)	XP_024308867.1:p.Gln14245Ter
XM_024453100.1:c.32587C>T (TTN)	XP_024308868.1:p.Gln10863Ter