Canonical Allele Identifier: CA349656727

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179500166C>G (hg19) ; chr2:g.178635439C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178635439C>G , CM000664.2:g.178635439C>G	GRCh38
NC_000002.11:g.179500166C>G , CM000664.1:g.179500166C>G	GRCh37
NC_000002.10:g.179208411C>G	NCBI36
NG_011618.3:g.200364G>C , LRG_391:g.200364G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.34180+1G>C	ENSP00000343764.6:n.34180+1G>C
ENST00000342175.11:c.15265+1G>C	ENSP00000340554.6:n.15265+1G>C
ENST00000359218.10:c.15064+1G>C	ENSP00000352154.5:n.15064+1G>C
ENST00000342175.10:c.15265+1G>C	ENSP00000340554.6:n.15265+1G>C
ENST00000342992.10:c.34180+1G>C	ENSP00000343764.6:n.34180+1G>C
ENST00000359218.9:c.15064+1G>C	ENSP00000352154.5:n.15064+1G>C
ENST00000460472.6:c.14689+1G>C	ENSP00000434586.1:n.14689+1G>C
ENST00000589042.5:c.41884+1G>C MANE Select	ENSP00000467141.1:n.41884+1G>C
ENST00000591111.5:c.36961+1G>C	ENSP00000465570.1:n.36961+1G>C
ENST00000615779.4:c.36961+1G>C	ENSP00000483597.1:n.36961+1G>C
NM_001256850.1:c.36961+1G>C	NP_001243779.1:n.36961+1G>C
NM_001267550.2:c.41884+1G>C MANE Select	NP_001254479.2:n.41884+1G>C
NM_003319.4:c.14689+1G>C	NP_003310.4:n.14689+1G>C
NM_133378.4:c.34180+1G>C	NP_596869.4:n.34180+1G>C
NM_133432.3:c.15064+1G>C	NP_597676.3:n.15064+1G>C
NM_133437.4:c.15265+1G>C	NP_597681.4:n.15265+1G>C
XM_011511729.1:c.40981+1G>C	XP_011510031.1:n.40981+1G>C
XM_011511730.1:c.14875+1G>C	XP_011510032.1:n.14875+1G>C
XM_011511731.1:c.14734+1G>C	XP_011510033.1:n.14734+1G>C
XM_017004819.1:c.40777+1G>C	XP_016860308.1:n.40777+1G>C
XM_017004820.1:c.36175+1G>C	XP_016860309.1:n.36175+1G>C
XM_017004821.1:c.36172+1G>C	XP_016860310.1:n.36172+1G>C
XM_017004822.1:c.33214+1G>C	XP_016860311.1:n.33214+1G>C
XM_017004823.1:c.14830+1G>C	XP_016860312.1:n.14830+1G>C
XM_024453094.1:c.36325+1G>C	XP_024308862.1:n.36325+1G>C
XM_024453095.1:c.36322+1G>C	XP_024308863.1:n.36322+1G>C
XM_024453096.1:c.35755+1G>C	XP_024308864.1:n.35755+1G>C
XM_024453097.1:c.33097+1G>C	XP_024308865.1:n.33097+1G>C
XM_024453098.1:c.33016+1G>C	XP_024308866.1:n.33016+1G>C
XM_024453099.1:c.14779+1G>C	XP_024308867.1:n.14779+1G>C
XM_024453100.1:c.4633+1G>C	XP_024308868.1:n.4633+1G>C