Canonical Allele Identifier: CA2662135795

Gene: TTN

Linked Data

• gnomAD v4: 2-178635325-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178635325G>A , CM000664.2:g.178635325G>A	GRCh38
NC_000002.11:g.179500052G>A , CM000664.1:g.179500052G>A	GRCh37
NC_000002.10:g.179208297G>A	NCBI36
NG_011618.3:g.200478C>T , LRG_391:g.200478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.34181-21C>T	ENSP00000343764.6:n.34181-21C>T
ENST00000342175.11:c.15266-21C>T	ENSP00000340554.6:n.15266-21C>T
ENST00000359218.10:c.15065-21C>T	ENSP00000352154.5:n.15065-21C>T
ENST00000342175.10:c.15266-21C>T	ENSP00000340554.6:n.15266-21C>T
ENST00000342992.10:c.34181-21C>T	ENSP00000343764.6:n.34181-21C>T
ENST00000359218.9:c.15065-21C>T	ENSP00000352154.5:n.15065-21C>T
ENST00000460472.6:c.14690-21C>T	ENSP00000434586.1:n.14690-21C>T
ENST00000589042.5:c.41885-21C>T MANE Select	ENSP00000467141.1:n.41885-21C>T
ENST00000591111.5:c.36962-21C>T	ENSP00000465570.1:n.36962-21C>T
ENST00000615779.4:c.36962-21C>T	ENSP00000483597.1:n.36962-21C>T
NM_001256850.1:c.36962-21C>T	NP_001243779.1:n.36962-21C>T
NM_001267550.2:c.41885-21C>T MANE Select	NP_001254479.2:n.41885-21C>T
NM_003319.4:c.14690-21C>T	NP_003310.4:n.14690-21C>T
NM_133378.4:c.34181-21C>T	NP_596869.4:n.34181-21C>T
NM_133432.3:c.15065-21C>T	NP_597676.3:n.15065-21C>T
NM_133437.4:c.15266-21C>T	NP_597681.4:n.15266-21C>T
XM_011511729.1:c.40982-21C>T	XP_011510031.1:n.40982-21C>T
XM_011511730.1:c.14876-21C>T	XP_011510032.1:n.14876-21C>T
XM_011511731.1:c.14735-21C>T	XP_011510033.1:n.14735-21C>T
XM_017004819.1:c.40778-21C>T	XP_016860308.1:n.40778-21C>T
XM_017004820.1:c.36176-21C>T	XP_016860309.1:n.36176-21C>T
XM_017004821.1:c.36173-21C>T	XP_016860310.1:n.36173-21C>T
XM_017004822.1:c.33215-21C>T	XP_016860311.1:n.33215-21C>T
XM_017004823.1:c.14831-21C>T	XP_016860312.1:n.14831-21C>T
XM_024453094.1:c.36326-21C>T	XP_024308862.1:n.36326-21C>T
XM_024453095.1:c.36323-21C>T	XP_024308863.1:n.36323-21C>T
XM_024453096.1:c.35756-21C>T	XP_024308864.1:n.35756-21C>T
XM_024453097.1:c.33098-21C>T	XP_024308865.1:n.33098-21C>T
XM_024453098.1:c.33017-21C>T	XP_024308866.1:n.33017-21C>T
XM_024453099.1:c.14780-21C>T	XP_024308867.1:n.14780-21C>T
XM_024453100.1:c.4634-21C>T	XP_024308868.1:n.4634-21C>T