Canonical Allele Identifier: CA349640306

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179489234C>A (hg19) ; chr2:g.178624507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178624507C>A , CM000664.2:g.178624507C>A	GRCh38
NC_000002.11:g.179489234C>A , CM000664.1:g.179489234C>A	GRCh37
NC_000002.10:g.179197479C>A	NCBI36
NG_011618.3:g.211296G>T , LRG_391:g.211296G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.37069G>T	ENSP00000343764.6:p.Asp12357Tyr
ENST00000342175.11:c.18154G>T	ENSP00000340554.6:p.Asp6052Tyr
ENST00000359218.10:c.17953G>T	ENSP00000352154.5:p.Asp5985Tyr
ENST00000342175.10:c.18154G>T	ENSP00000340554.6:p.Asp6052Tyr
ENST00000342992.10:c.37069G>T	ENSP00000343764.6:p.Asp12357Tyr
ENST00000359218.9:c.17953G>T	ENSP00000352154.5:p.Asp5985Tyr
ENST00000460472.6:c.17578G>T	ENSP00000434586.1:p.Asp5860Tyr
ENST00000589042.5:c.44773G>T MANE Select	ENSP00000467141.1:p.Asp14925Tyr
ENST00000591111.5:c.39850G>T	ENSP00000465570.1:p.Asp13284Tyr
ENST00000615779.4:c.39850G>T	ENSP00000483597.1:p.Asp13284Tyr
NM_001256850.1:c.39850G>T	NP_001243779.1:p.Asp13284Tyr
NM_001267550.2:c.44773G>T MANE Select	NP_001254479.2:p.Asp14925Tyr
NM_003319.4:c.17578G>T	NP_003310.4:p.Asp5860Tyr
NM_133378.4:c.37069G>T	NP_596869.4:p.Asp12357Tyr
NM_133432.3:c.17953G>T	NP_597676.3:p.Asp5985Tyr
NM_133437.4:c.18154G>T	NP_597681.4:p.Asp6052Tyr
XM_011511729.1:c.43870G>T	XP_011510031.1:p.Asp14624Tyr
XM_011511730.1:c.17764G>T	XP_011510032.1:p.Asp5922Tyr
XM_011511731.1:c.17623G>T	XP_011510033.1:p.Asp5875Tyr
XM_017004819.1:c.43666G>T	XP_016860308.1:p.Asp14556Tyr
XM_017004820.1:c.39064G>T	XP_016860309.1:p.Asp13022Tyr
XM_017004821.1:c.39061G>T	XP_016860310.1:p.Asp13021Tyr
XM_017004822.1:c.36103G>T	XP_016860311.1:p.Asp12035Tyr
XM_017004823.1:c.17719G>T	XP_016860312.1:p.Asp5907Tyr
XM_024453094.1:c.39214G>T	XP_024308862.1:p.Asp13072Tyr
XM_024453095.1:c.39211G>T	XP_024308863.1:p.Asp13071Tyr
XM_024453096.1:c.38644G>T	XP_024308864.1:p.Asp12882Tyr
XM_024453097.1:c.35986G>T	XP_024308865.1:p.Asp11996Tyr
XM_024453098.1:c.35905G>T	XP_024308866.1:p.Asp11969Tyr
XM_024453099.1:c.17668G>T	XP_024308867.1:p.Asp5890Tyr
XM_024453100.1:c.7522G>T	XP_024308868.1:p.Asp2508Tyr