Canonical Allele Identifier: CA349411858

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396959T>C (hg19) ; chr2:g.178532232T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532232T>C , CM000664.2:g.178532232T>C	GRCh38
NC_000002.11:g.179396959T>C , CM000664.1:g.179396959T>C	GRCh37
NC_000002.10:g.179105205T>C	NCBI36
NG_011618.3:g.303571A>G , LRG_391:g.303571A>G
NG_051363.1:g.14406T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96679A>G (TTN)	ENSP00000343764.6:p.Lys32227Glu
ENST00000342175.11:c.77764A>G (TTN)	ENSP00000340554.6:p.Lys25922Glu
ENST00000359218.10:c.77563A>G (TTN)	ENSP00000352154.5:p.Lys25855Glu
ENST00000342175.10:c.77764A>G (TTN)	ENSP00000340554.6:p.Lys25922Glu
ENST00000342992.10:c.96679A>G (TTN)	ENSP00000343764.6:p.Lys32227Glu
ENST00000359218.9:c.77563A>G (TTN)	ENSP00000352154.5:p.Lys25855Glu
ENST00000460472.6:c.77188A>G (TTN)	ENSP00000434586.1:p.Lys25730Glu
ENST00000589042.5:c.104383A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys34795Glu
ENST00000591111.5:c.99460A>G (TTN)	ENSP00000465570.1:p.Lys33154Glu
ENST00000615779.4:c.99460A>G (TTN)	ENSP00000483597.1:p.Lys33154Glu
NM_001256850.1:c.99460A>G (TTN)	NP_001243779.1:p.Lys33154Glu
NM_001267550.2:c.104383A>G (TTN) MANE Select	NP_001254479.2:p.Lys34795Glu
NM_003319.4:c.77188A>G (TTN)	NP_003310.4:p.Lys25730Glu
NM_133378.4:c.96679A>G (TTN)	NP_596869.4:p.Lys32227Glu
NM_133432.3:c.77563A>G (TTN)	NP_597676.3:p.Lys25855Glu
NM_133437.4:c.77764A>G (TTN)	NP_597681.4:p.Lys25922Glu
NR_038271.1:n.446+8596T>C (TTN-AS1)
NR_038272.1:n.220-3500T>C (TTN-AS1)
XM_011511729.1:c.103480A>G (TTN)	XP_011510031.1:p.Lys34494Glu
XM_011511730.1:c.77374A>G (TTN)	XP_011510032.1:p.Lys25792Glu
XM_011511731.1:c.77233A>G (TTN)	XP_011510033.1:p.Lys25745Glu
XM_017004819.1:c.103276A>G (TTN)	XP_016860308.1:p.Lys34426Glu
XM_017004820.1:c.98674A>G (TTN)	XP_016860309.1:p.Lys32892Glu
XM_017004821.1:c.98671A>G (TTN)	XP_016860310.1:p.Lys32891Glu
XM_017004822.1:c.95713A>G (TTN)	XP_016860311.1:p.Lys31905Glu
XM_017004823.1:c.77329A>G (TTN)	XP_016860312.1:p.Lys25777Glu
XM_024453094.1:c.98824A>G (TTN)	XP_024308862.1:p.Lys32942Glu
XM_024453095.1:c.98821A>G (TTN)	XP_024308863.1:p.Lys32941Glu
XM_024453096.1:c.98254A>G (TTN)	XP_024308864.1:p.Lys32752Glu
XM_024453097.1:c.95596A>G (TTN)	XP_024308865.1:p.Lys31866Glu
XM_024453098.1:c.95515A>G (TTN)	XP_024308866.1:p.Lys31839Glu
XM_024453099.1:c.77278A>G (TTN)	XP_024308867.1:p.Lys25760Glu
XM_024453100.1:c.67132A>G (TTN)	XP_024308868.1:p.Lys22378Glu