Canonical Allele Identifier: CA1987208

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547573C>T , CM000664.2:g.178547573C>T	GRCh38
NC_000002.11:g.179412300C>T , CM000664.1:g.179412300C>T	GRCh37
NC_000002.10:g.179120546C>T	NCBI36
NG_011618.3:g.288230G>A , LRG_391:g.288230G>A
NG_051363.1:g.29747C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.94053G>A (TTN) MANE Select	NP_001254479.2:p.Ser31351=
ENST00000589042.5:c.94053G>A (TTN) MANE Select	ENSP00000467141.1:p.Ser31351=
NM_001256850.1:c.89130G>A (TTN)	NP_001243779.1:p.Ser29710=
NM_003319.4:c.66858G>A (TTN)	NP_003310.4:p.Ser22286=
NM_133378.4:c.86349G>A (TTN)	NP_596869.4:p.Ser28783=
NM_133432.3:c.67233G>A (TTN)	NP_597676.3:p.Ser22411=
NM_133437.4:c.67434G>A (TTN)	NP_597681.4:p.Ser22478=
NR_038271.1:n.447-23727C>T (TTN-AS1)
NR_038272.1:n.2043+5212C>T (TTN-AS1)
ENST00000342175.10:c.67434G>A (TTN)	ENSP00000340554.6:p.Ser22478=
ENST00000342175.11:c.67434G>A (TTN)	ENSP00000340554.6:p.Ser22478=
ENST00000342992.10:c.86349G>A (TTN)	ENSP00000343764.6:p.Ser28783=
ENST00000342992.11:c.86349G>A (TTN)	ENSP00000343764.6:p.Ser28783=
ENST00000359218.10:c.67233G>A (TTN)	ENSP00000352154.5:p.Ser22411=
ENST00000359218.9:c.67233G>A (TTN)	ENSP00000352154.5:p.Ser22411=
ENST00000460472.6:c.66858G>A (TTN)	ENSP00000434586.1:p.Ser22286=
ENST00000591111.5:c.89130G>A (TTN)	ENSP00000465570.1:p.Ser29710=
ENST00000615779.4:c.89130G>A (TTN)	ENSP00000483597.1:p.Ser29710=
XM_011511729.1:c.93150G>A (TTN)	XP_011510031.1:p.Ser31050=
XM_011511730.1:c.67044G>A (TTN)	XP_011510032.1:p.Ser22348=
XM_011511731.1:c.66903G>A (TTN)	XP_011510033.1:p.Ser22301=
XM_017004819.1:c.92946G>A (TTN)	XP_016860308.1:p.Ser30982=
XM_017004820.1:c.88344G>A (TTN)	XP_016860309.1:p.Ser29448=
XM_017004821.1:c.88341G>A (TTN)	XP_016860310.1:p.Ser29447=
XM_017004822.1:c.85383G>A (TTN)	XP_016860311.1:p.Ser28461=
XM_017004823.1:c.66999G>A (TTN)	XP_016860312.1:p.Ser22333=
XM_024453094.1:c.88494G>A (TTN)	XP_024308862.1:p.Ser29498=
XM_024453095.1:c.88491G>A (TTN)	XP_024308863.1:p.Ser29497=
XM_024453096.1:c.87924G>A (TTN)	XP_024308864.1:p.Ser29308=
XM_024453097.1:c.85266G>A (TTN)	XP_024308865.1:p.Ser28422=
XM_024453098.1:c.85185G>A (TTN)	XP_024308866.1:p.Ser28395=
XM_024453099.1:c.66948G>A (TTN)	XP_024308867.1:p.Ser22316=
XM_024453100.1:c.56802G>A (TTN)	XP_024308868.1:p.Ser18934=