Canonical Allele Identifier: CA349411843

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396954C>A (hg19) ; chr2:g.178532227C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532227C>A , CM000664.2:g.178532227C>A	GRCh38
NC_000002.11:g.179396954C>A , CM000664.1:g.179396954C>A	GRCh37
NC_000002.10:g.179105200C>A	NCBI36
NG_011618.3:g.303576G>T , LRG_391:g.303576G>T
NG_051363.1:g.14401C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96684G>T (TTN)	ENSP00000343764.6:p.Glu32228Asp
ENST00000342175.11:c.77769G>T (TTN)	ENSP00000340554.6:p.Glu25923Asp
ENST00000359218.10:c.77568G>T (TTN)	ENSP00000352154.5:p.Glu25856Asp
ENST00000342175.10:c.77769G>T (TTN)	ENSP00000340554.6:p.Glu25923Asp
ENST00000342992.10:c.96684G>T (TTN)	ENSP00000343764.6:p.Glu32228Asp
ENST00000359218.9:c.77568G>T (TTN)	ENSP00000352154.5:p.Glu25856Asp
ENST00000460472.6:c.77193G>T (TTN)	ENSP00000434586.1:p.Glu25731Asp
ENST00000589042.5:c.104388G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu34796Asp
ENST00000591111.5:c.99465G>T (TTN)	ENSP00000465570.1:p.Glu33155Asp
ENST00000615779.4:c.99465G>T (TTN)	ENSP00000483597.1:p.Glu33155Asp
NM_001256850.1:c.99465G>T (TTN)	NP_001243779.1:p.Glu33155Asp
NM_001267550.2:c.104388G>T (TTN) MANE Select	NP_001254479.2:p.Glu34796Asp
NM_003319.4:c.77193G>T (TTN)	NP_003310.4:p.Glu25731Asp
NM_133378.4:c.96684G>T (TTN)	NP_596869.4:p.Glu32228Asp
NM_133432.3:c.77568G>T (TTN)	NP_597676.3:p.Glu25856Asp
NM_133437.4:c.77769G>T (TTN)	NP_597681.4:p.Glu25923Asp
NR_038271.1:n.446+8591C>A (TTN-AS1)
NR_038272.1:n.220-3505C>A (TTN-AS1)
XM_011511729.1:c.103485G>T (TTN)	XP_011510031.1:p.Glu34495Asp
XM_011511730.1:c.77379G>T (TTN)	XP_011510032.1:p.Glu25793Asp
XM_011511731.1:c.77238G>T (TTN)	XP_011510033.1:p.Glu25746Asp
XM_017004819.1:c.103281G>T (TTN)	XP_016860308.1:p.Glu34427Asp
XM_017004820.1:c.98679G>T (TTN)	XP_016860309.1:p.Glu32893Asp
XM_017004821.1:c.98676G>T (TTN)	XP_016860310.1:p.Glu32892Asp
XM_017004822.1:c.95718G>T (TTN)	XP_016860311.1:p.Glu31906Asp
XM_017004823.1:c.77334G>T (TTN)	XP_016860312.1:p.Glu25778Asp
XM_024453094.1:c.98829G>T (TTN)	XP_024308862.1:p.Glu32943Asp
XM_024453095.1:c.98826G>T (TTN)	XP_024308863.1:p.Glu32942Asp
XM_024453096.1:c.98259G>T (TTN)	XP_024308864.1:p.Glu32753Asp
XM_024453097.1:c.95601G>T (TTN)	XP_024308865.1:p.Glu31867Asp
XM_024453098.1:c.95520G>T (TTN)	XP_024308866.1:p.Glu31840Asp
XM_024453099.1:c.77283G>T (TTN)	XP_024308867.1:p.Glu25761Asp
XM_024453100.1:c.67137G>T (TTN)	XP_024308868.1:p.Glu22379Asp