Canonical Allele Identifier: CA2662135821

Gene: TTN

Linked Data

• gnomAD v4: 2-178635356-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178635356C>T , CM000664.2:g.178635356C>T	GRCh38
NC_000002.11:g.179500083C>T , CM000664.1:g.179500083C>T	GRCh37
NC_000002.10:g.179208328C>T	NCBI36
NG_011618.3:g.200447G>A , LRG_391:g.200447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.34181-52G>A	ENSP00000343764.6:n.34181-52G>A
ENST00000342175.11:c.15266-52G>A	ENSP00000340554.6:n.15266-52G>A
ENST00000359218.10:c.15065-52G>A	ENSP00000352154.5:n.15065-52G>A
ENST00000342175.10:c.15266-52G>A	ENSP00000340554.6:n.15266-52G>A
ENST00000342992.10:c.34181-52G>A	ENSP00000343764.6:n.34181-52G>A
ENST00000359218.9:c.15065-52G>A	ENSP00000352154.5:n.15065-52G>A
ENST00000460472.6:c.14690-52G>A	ENSP00000434586.1:n.14690-52G>A
ENST00000589042.5:c.41885-52G>A MANE Select	ENSP00000467141.1:n.41885-52G>A
ENST00000591111.5:c.36962-52G>A	ENSP00000465570.1:n.36962-52G>A
ENST00000615779.4:c.36962-52G>A	ENSP00000483597.1:n.36962-52G>A
NM_001256850.1:c.36962-52G>A	NP_001243779.1:n.36962-52G>A
NM_001267550.2:c.41885-52G>A MANE Select	NP_001254479.2:n.41885-52G>A
NM_003319.4:c.14690-52G>A	NP_003310.4:n.14690-52G>A
NM_133378.4:c.34181-52G>A	NP_596869.4:n.34181-52G>A
NM_133432.3:c.15065-52G>A	NP_597676.3:n.15065-52G>A
NM_133437.4:c.15266-52G>A	NP_597681.4:n.15266-52G>A
XM_011511729.1:c.40982-52G>A	XP_011510031.1:n.40982-52G>A
XM_011511730.1:c.14876-52G>A	XP_011510032.1:n.14876-52G>A
XM_011511731.1:c.14735-52G>A	XP_011510033.1:n.14735-52G>A
XM_017004819.1:c.40778-52G>A	XP_016860308.1:n.40778-52G>A
XM_017004820.1:c.36176-52G>A	XP_016860309.1:n.36176-52G>A
XM_017004821.1:c.36173-52G>A	XP_016860310.1:n.36173-52G>A
XM_017004822.1:c.33215-52G>A	XP_016860311.1:n.33215-52G>A
XM_017004823.1:c.14831-52G>A	XP_016860312.1:n.14831-52G>A
XM_024453094.1:c.36326-52G>A	XP_024308862.1:n.36326-52G>A
XM_024453095.1:c.36323-52G>A	XP_024308863.1:n.36323-52G>A
XM_024453096.1:c.35756-52G>A	XP_024308864.1:n.35756-52G>A
XM_024453097.1:c.33098-52G>A	XP_024308865.1:n.33098-52G>A
XM_024453098.1:c.33017-52G>A	XP_024308866.1:n.33017-52G>A
XM_024453099.1:c.14780-52G>A	XP_024308867.1:n.14780-52G>A
XM_024453100.1:c.4634-52G>A	XP_024308868.1:n.4634-52G>A