Canonical Allele Identifier: CA1998008

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178674326C>A , CM000664.2:g.178674326C>A	GRCh38
NC_000002.11:g.179539053C>A , CM000664.1:g.179539053C>A	GRCh37
NC_000002.10:g.179247298C>A	NCBI36
NG_011618.3:g.161477G>T , LRG_391:g.161477G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.34696G>T MANE Select	NP_001254479.2:p.Ala11566Ser
ENST00000589042.5:c.34696G>T MANE Select	ENSP00000467141.1:p.Ala11566Ser
NM_001256850.1:c.33574G>T	NP_001243779.1:p.Ala11192Ser
NM_003319.4:c.13283-32009G>T	NP_003310.4:n.13283-32009G>T
NM_133378.4:c.30793G>T	NP_596869.4:p.Ala10265Ser
NM_133432.3:c.13658-32009G>T	NP_597676.3:n.13658-32009G>T
NM_133437.4:c.13859-32009G>T	NP_597681.4:n.13859-32009G>T
ENST00000342175.10:c.13859-32009G>T	ENSP00000340554.6:n.13859-32009G>T
ENST00000342175.11:c.13859-32009G>T	ENSP00000340554.6:n.13859-32009G>T
ENST00000342992.10:c.30793G>T	ENSP00000343764.6:p.Ala10265Ser
ENST00000342992.11:c.30793G>T	ENSP00000343764.6:p.Ala10265Ser
ENST00000359218.10:c.13658-32009G>T	ENSP00000352154.5:n.13658-32009G>T
ENST00000359218.9:c.13658-32009G>T	ENSP00000352154.5:n.13658-32009G>T
ENST00000414766.5:c.2350G>T	ENSP00000401501.1:p.Ala784Ser
ENST00000460472.6:c.13283-32009G>T	ENSP00000434586.1:n.13283-32009G>T
ENST00000591111.5:c.33574G>T	ENSP00000465570.1:p.Ala11192Ser
ENST00000615779.4:c.33574G>T	ENSP00000483597.1:p.Ala11192Ser
XM_011511729.1:c.33793G>T	XP_011510031.1:p.Ala11265Ser
XM_011511730.1:c.13469-32009G>T	XP_011510032.1:n.13469-32009G>T
XM_011511731.1:c.13328-32009G>T	XP_011510033.1:n.13328-32009G>T
XM_017004819.1:c.33748G>T	XP_016860308.1:p.Ala11250Ser
XM_017004820.1:c.30796G>T	XP_016860309.1:p.Ala10266Ser
XM_017004821.1:c.30793G>T	XP_016860310.1:p.Ala10265Ser
XM_017004822.1:c.31768G>T	XP_016860311.1:p.Ala10590Ser
XM_017004823.1:c.13424-32009G>T	XP_016860312.1:n.13424-32009G>T
XM_024453094.1:c.33130G>T	XP_024308862.1:p.Ala11044Ser
XM_024453095.1:c.33205G>T	XP_024308863.1:p.Ala11069Ser
XM_024453096.1:c.32560G>T	XP_024308864.1:p.Ala10854Ser
XM_024453097.1:c.31600G>T	XP_024308865.1:p.Ala10534Ser
XM_024453098.1:c.31519G>T	XP_024308866.1:p.Ala10507Ser
XM_024453099.1:c.13424-32009G>T	XP_024308867.1:n.13424-32009G>T