Canonical Allele Identifier: CA349614030

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178617446C>T , CM000664.2:g.178617446C>T	GRCh38
NC_000002.11:g.179482173C>T , CM000664.1:g.179482173C>T	GRCh37
NC_000002.10:g.179190418C>T	NCBI36
NG_011618.3:g.218357G>A , LRG_391:g.218357G>A
NG_051363.1:g.99620C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.47639G>A (TTN) MANE Select	NP_001254479.2:p.Trp15880Ter
ENST00000589042.5:c.47639G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp15880Ter
NM_001256850.1:c.42716G>A (TTN)	NP_001243779.1:p.Trp14239Ter
NM_003319.4:c.20444G>A (TTN)	NP_003310.4:p.Trp6815Ter
NM_133378.4:c.39935G>A (TTN)	NP_596869.4:p.Trp13312Ter
NM_133432.3:c.20819G>A (TTN)	NP_597676.3:p.Trp6940Ter
NM_133437.4:c.21020G>A (TTN)	NP_597681.4:p.Trp7007Ter
NR_038271.1:n.1604+2072C>T (TTN-AS1)
ENST00000342175.10:c.21020G>A (TTN)	ENSP00000340554.6:p.Trp7007Ter
ENST00000342175.11:c.21020G>A (TTN)	ENSP00000340554.6:p.Trp7007Ter
ENST00000342992.10:c.39935G>A (TTN)	ENSP00000343764.6:p.Trp13312Ter
ENST00000342992.11:c.39935G>A (TTN)	ENSP00000343764.6:p.Trp13312Ter
ENST00000359218.10:c.20819G>A (TTN)	ENSP00000352154.5:p.Trp6940Ter
ENST00000359218.9:c.20819G>A (TTN)	ENSP00000352154.5:p.Trp6940Ter
ENST00000460472.6:c.20444G>A (TTN)	ENSP00000434586.1:p.Trp6815Ter
ENST00000591111.5:c.42716G>A (TTN)	ENSP00000465570.1:p.Trp14239Ter
ENST00000615779.4:c.42716G>A (TTN)	ENSP00000483597.1:p.Trp14239Ter
XM_011511729.1:c.46736G>A (TTN)	XP_011510031.1:p.Trp15579Ter
XM_011511730.1:c.20630G>A (TTN)	XP_011510032.1:p.Trp6877Ter
XM_011511731.1:c.20489G>A (TTN)	XP_011510033.1:p.Trp6830Ter
XM_017004819.1:c.46532G>A (TTN)	XP_016860308.1:p.Trp15511Ter
XM_017004820.1:c.41930G>A (TTN)	XP_016860309.1:p.Trp13977Ter
XM_017004821.1:c.41927G>A (TTN)	XP_016860310.1:p.Trp13976Ter
XM_017004822.1:c.38969G>A (TTN)	XP_016860311.1:p.Trp12990Ter
XM_017004823.1:c.20585G>A (TTN)	XP_016860312.1:p.Trp6862Ter
XM_024453094.1:c.42080G>A (TTN)	XP_024308862.1:p.Trp14027Ter
XM_024453095.1:c.42077G>A (TTN)	XP_024308863.1:p.Trp14026Ter
XM_024453096.1:c.41510G>A (TTN)	XP_024308864.1:p.Trp13837Ter
XM_024453097.1:c.38852G>A (TTN)	XP_024308865.1:p.Trp12951Ter
XM_024453098.1:c.38771G>A (TTN)	XP_024308866.1:p.Trp12924Ter
XM_024453099.1:c.20534G>A (TTN)	XP_024308867.1:p.Trp6845Ter
XM_024453100.1:c.10388G>A (TTN)	XP_024308868.1:p.Trp3463Ter