Canonical Allele Identifier: CA430235895

Linked Data

MyVariant Identifiers: chr2:g.179396873T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532146T>C , CM000664.2:g.178532146T>C GRCh38
NC_000002.11:g.179396873T>C , CM000664.1:g.179396873T>C GRCh37
NC_000002.10:g.179105119T>C NCBI36
NG_011618.3:g.303657A>G , LRG_391:g.303657A>G
NG_051363.1:g.14320T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96765A>G (TTN) ENSP00000343764.6:p.Lys32255=
ENST00000342175.11:c.77850A>G (TTN) ENSP00000340554.6:p.Lys25950=
ENST00000359218.10:c.77649A>G (TTN) ENSP00000352154.5:p.Lys25883=
ENST00000342175.10:c.77850A>G (TTN) ENSP00000340554.6:p.Lys25950=
ENST00000342992.10:c.96765A>G (TTN) ENSP00000343764.6:p.Lys32255=
ENST00000359218.9:c.77649A>G (TTN) ENSP00000352154.5:p.Lys25883=
ENST00000460472.6:c.77274A>G (TTN) ENSP00000434586.1:p.Lys25758=
ENST00000589042.5:c.104469A>G (TTN) MANE Select ENSP00000467141.1:p.Lys34823=
ENST00000591111.5:c.99546A>G (TTN) ENSP00000465570.1:p.Lys33182=
ENST00000615779.4:c.99546A>G (TTN) ENSP00000483597.1:p.Lys33182=
NM_001256850.1:c.99546A>G (TTN) NP_001243779.1:p.Lys33182=
NM_001267550.2:c.104469A>G (TTN) MANE Select NP_001254479.2:p.Lys34823=
NM_003319.4:c.77274A>G (TTN) NP_003310.4:p.Lys25758=
NM_133378.4:c.96765A>G (TTN) NP_596869.4:p.Lys32255=
NM_133432.3:c.77649A>G (TTN) NP_597676.3:p.Lys25883=
NM_133437.4:c.77850A>G (TTN) NP_597681.4:p.Lys25950=
NR_038271.1:n.446+8510T>C (TTN-AS1)
NR_038272.1:n.220-3586T>C (TTN-AS1)
XM_011511729.1:c.103566A>G (TTN) XP_011510031.1:p.Lys34522=
XM_011511730.1:c.77460A>G (TTN) XP_011510032.1:p.Lys25820=
XM_011511731.1:c.77319A>G (TTN) XP_011510033.1:p.Lys25773=
XM_017004819.1:c.103362A>G (TTN) XP_016860308.1:p.Lys34454=
XM_017004820.1:c.98760A>G (TTN) XP_016860309.1:p.Lys32920=
XM_017004821.1:c.98757A>G (TTN) XP_016860310.1:p.Lys32919=
XM_017004822.1:c.95799A>G (TTN) XP_016860311.1:p.Lys31933=
XM_017004823.1:c.77415A>G (TTN) XP_016860312.1:p.Lys25805=
XM_024453094.1:c.98910A>G (TTN) XP_024308862.1:p.Lys32970=
XM_024453095.1:c.98907A>G (TTN) XP_024308863.1:p.Lys32969=
XM_024453096.1:c.98340A>G (TTN) XP_024308864.1:p.Lys32780=
XM_024453097.1:c.95682A>G (TTN) XP_024308865.1:p.Lys31894=
XM_024453098.1:c.95601A>G (TTN) XP_024308866.1:p.Lys31867=
XM_024453099.1:c.77364A>G (TTN) XP_024308867.1:p.Lys25788=
XM_024453100.1:c.67218A>G (TTN) XP_024308868.1:p.Lys22406=