Canonical Allele Identifier: CA349434918

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179404807T>A (hg19) ; chr2:g.178540080T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178540080T>A , CM000664.2:g.178540080T>A	GRCh38
NC_000002.11:g.179404807T>A , CM000664.1:g.179404807T>A	GRCh37
NC_000002.10:g.179113053T>A	NCBI36
NG_011618.3:g.295723A>T , LRG_391:g.295723A>T
NG_051363.1:g.22254T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.90382A>T (TTN)	ENSP00000343764.6:p.Thr30128Ser
ENST00000342175.11:c.71467A>T (TTN)	ENSP00000340554.6:p.Thr23823Ser
ENST00000359218.10:c.71266A>T (TTN)	ENSP00000352154.5:p.Thr23756Ser
ENST00000342175.10:c.71467A>T (TTN)	ENSP00000340554.6:p.Thr23823Ser
ENST00000342992.10:c.90382A>T (TTN)	ENSP00000343764.6:p.Thr30128Ser
ENST00000359218.9:c.71266A>T (TTN)	ENSP00000352154.5:p.Thr23756Ser
ENST00000460472.6:c.70891A>T (TTN)	ENSP00000434586.1:p.Thr23631Ser
ENST00000589042.5:c.98086A>T (TTN) MANE Select	ENSP00000467141.1:p.Thr32696Ser
ENST00000591111.5:c.93163A>T (TTN)	ENSP00000465570.1:p.Thr31055Ser
ENST00000615779.4:c.93163A>T (TTN)	ENSP00000483597.1:p.Thr31055Ser
NM_001256850.1:c.93163A>T (TTN)	NP_001243779.1:p.Thr31055Ser
NM_001267550.2:c.98086A>T (TTN) MANE Select	NP_001254479.2:p.Thr32696Ser
NM_003319.4:c.70891A>T (TTN)	NP_003310.4:p.Thr23631Ser
NM_133378.4:c.90382A>T (TTN)	NP_596869.4:p.Thr30128Ser
NM_133432.3:c.71266A>T (TTN)	NP_597676.3:p.Thr23756Ser
NM_133437.4:c.71467A>T (TTN)	NP_597681.4:p.Thr23823Ser
NR_038271.1:n.446+16444T>A (TTN-AS1)
NR_038272.1:n.1841-27T>A (TTN-AS1)
XM_011511729.1:c.97183A>T (TTN)	XP_011510031.1:p.Thr32395Ser
XM_011511730.1:c.71077A>T (TTN)	XP_011510032.1:p.Thr23693Ser
XM_011511731.1:c.70936A>T (TTN)	XP_011510033.1:p.Thr23646Ser
XM_017004819.1:c.96979A>T (TTN)	XP_016860308.1:p.Thr32327Ser
XM_017004820.1:c.92377A>T (TTN)	XP_016860309.1:p.Thr30793Ser
XM_017004821.1:c.92374A>T (TTN)	XP_016860310.1:p.Thr30792Ser
XM_017004822.1:c.89416A>T (TTN)	XP_016860311.1:p.Thr29806Ser
XM_017004823.1:c.71032A>T (TTN)	XP_016860312.1:p.Thr23678Ser
XM_024453094.1:c.92527A>T (TTN)	XP_024308862.1:p.Thr30843Ser
XM_024453095.1:c.92524A>T (TTN)	XP_024308863.1:p.Thr30842Ser
XM_024453096.1:c.91957A>T (TTN)	XP_024308864.1:p.Thr30653Ser
XM_024453097.1:c.89299A>T (TTN)	XP_024308865.1:p.Thr29767Ser
XM_024453098.1:c.89218A>T (TTN)	XP_024308866.1:p.Thr29740Ser
XM_024453099.1:c.70981A>T (TTN)	XP_024308867.1:p.Thr23661Ser
XM_024453100.1:c.60835A>T (TTN)	XP_024308868.1:p.Thr20279Ser