Canonical Allele Identifier: CA430276964

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179497700T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178632973T>C , CM000664.2:g.178632973T>C	GRCh38
NC_000002.11:g.179497700T>C , CM000664.1:g.179497700T>C	GRCh37
NC_000002.10:g.179205945T>C	NCBI36
NG_011618.3:g.202830A>G , LRG_391:g.202830A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.35454A>G	ENSP00000343764.6:p.Gly11818=
ENST00000342175.11:c.16539A>G	ENSP00000340554.6:p.Gly5513=
ENST00000359218.10:c.16338A>G	ENSP00000352154.5:p.Gly5446=
ENST00000342175.10:c.16539A>G	ENSP00000340554.6:p.Gly5513=
ENST00000342992.10:c.35454A>G	ENSP00000343764.6:p.Gly11818=
ENST00000359218.9:c.16338A>G	ENSP00000352154.5:p.Gly5446=
ENST00000460472.6:c.15963A>G	ENSP00000434586.1:p.Gly5321=
ENST00000589042.5:c.43158A>G MANE Select	ENSP00000467141.1:p.Gly14386=
ENST00000591111.5:c.38235A>G	ENSP00000465570.1:p.Gly12745=
ENST00000615779.4:c.38235A>G	ENSP00000483597.1:p.Gly12745=
NM_001256850.1:c.38235A>G	NP_001243779.1:p.Gly12745=
NM_001267550.2:c.43158A>G MANE Select	NP_001254479.2:p.Gly14386=
NM_003319.4:c.15963A>G	NP_003310.4:p.Gly5321=
NM_133378.4:c.35454A>G	NP_596869.4:p.Gly11818=
NM_133432.3:c.16338A>G	NP_597676.3:p.Gly5446=
NM_133437.4:c.16539A>G	NP_597681.4:p.Gly5513=
XM_011511729.1:c.42255A>G	XP_011510031.1:p.Gly14085=
XM_011511730.1:c.16149A>G	XP_011510032.1:p.Gly5383=
XM_011511731.1:c.16008A>G	XP_011510033.1:p.Gly5336=
XM_017004819.1:c.42051A>G	XP_016860308.1:p.Gly14017=
XM_017004820.1:c.37449A>G	XP_016860309.1:p.Gly12483=
XM_017004821.1:c.37446A>G	XP_016860310.1:p.Gly12482=
XM_017004822.1:c.34488A>G	XP_016860311.1:p.Gly11496=
XM_017004823.1:c.16104A>G	XP_016860312.1:p.Gly5368=
XM_024453094.1:c.37599A>G	XP_024308862.1:p.Gly12533=
XM_024453095.1:c.37596A>G	XP_024308863.1:p.Gly12532=
XM_024453096.1:c.37029A>G	XP_024308864.1:p.Gly12343=
XM_024453097.1:c.34371A>G	XP_024308865.1:p.Gly11457=
XM_024453098.1:c.34290A>G	XP_024308866.1:p.Gly11430=
XM_024453099.1:c.16053A>G	XP_024308867.1:p.Gly5351=
XM_024453100.1:c.5907A>G	XP_024308868.1:p.Gly1969=