Canonical Allele Identifier: CA430253068

Linked Data

MyVariant Identifiers: chr2:g.179432025T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178567298T>C , CM000664.2:g.178567298T>C GRCh38
NC_000002.11:g.179432025T>C , CM000664.1:g.179432025T>C GRCh37
NC_000002.10:g.179140271T>C NCBI36
NG_011618.3:g.268505A>G , LRG_391:g.268505A>G
NG_051363.1:g.49472T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.71130A>G (TTN) ENSP00000343764.6:p.Pro23710=
ENST00000342175.11:c.52215A>G (TTN) ENSP00000340554.6:p.Pro17405=
ENST00000359218.10:c.52014A>G (TTN) ENSP00000352154.5:p.Pro17338=
ENST00000342175.10:c.52215A>G (TTN) ENSP00000340554.6:p.Pro17405=
ENST00000342992.10:c.71130A>G (TTN) ENSP00000343764.6:p.Pro23710=
ENST00000359218.9:c.52014A>G (TTN) ENSP00000352154.5:p.Pro17338=
ENST00000460472.6:c.51639A>G (TTN) ENSP00000434586.1:p.Pro17213=
ENST00000589042.5:c.78834A>G (TTN) MANE Select ENSP00000467141.1:p.Pro26278=
ENST00000591111.5:c.73911A>G (TTN) ENSP00000465570.1:p.Pro24637=
ENST00000615779.4:c.73911A>G (TTN) ENSP00000483597.1:p.Pro24637=
NM_001256850.1:c.73911A>G (TTN) NP_001243779.1:p.Pro24637=
NM_001267550.2:c.78834A>G (TTN) MANE Select NP_001254479.2:p.Pro26278=
NM_003319.4:c.51639A>G (TTN) NP_003310.4:p.Pro17213=
NM_133378.4:c.71130A>G (TTN) NP_596869.4:p.Pro23710=
NM_133432.3:c.52014A>G (TTN) NP_597676.3:p.Pro17338=
NM_133437.4:c.52215A>G (TTN) NP_597681.4:p.Pro17405=
NR_038271.1:n.447-4002T>C (TTN-AS1)
NR_038272.1:n.2044-15274T>C (TTN-AS1)
XM_011511729.1:c.77931A>G (TTN) XP_011510031.1:p.Pro25977=
XM_011511730.1:c.51825A>G (TTN) XP_011510032.1:p.Pro17275=
XM_011511731.1:c.51684A>G (TTN) XP_011510033.1:p.Pro17228=
XM_017004819.1:c.77727A>G (TTN) XP_016860308.1:p.Pro25909=
XM_017004820.1:c.73125A>G (TTN) XP_016860309.1:p.Pro24375=
XM_017004821.1:c.73122A>G (TTN) XP_016860310.1:p.Pro24374=
XM_017004822.1:c.70164A>G (TTN) XP_016860311.1:p.Pro23388=
XM_017004823.1:c.51780A>G (TTN) XP_016860312.1:p.Pro17260=
XM_024453094.1:c.73275A>G (TTN) XP_024308862.1:p.Pro24425=
XM_024453095.1:c.73272A>G (TTN) XP_024308863.1:p.Pro24424=
XM_024453096.1:c.72705A>G (TTN) XP_024308864.1:p.Pro24235=
XM_024453097.1:c.70047A>G (TTN) XP_024308865.1:p.Pro23349=
XM_024453098.1:c.69966A>G (TTN) XP_024308866.1:p.Pro23322=
XM_024453099.1:c.51729A>G (TTN) XP_024308867.1:p.Pro17243=
XM_024453100.1:c.41583A>G (TTN) XP_024308868.1:p.Pro13861=