Canonical Allele Identifier: CA349661764

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501439G>T (hg19) ; chr2:g.178636712G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636712G>T , CM000664.2:g.178636712G>T	GRCh38
NC_000002.11:g.179501439G>T , CM000664.1:g.179501439G>T	GRCh37
NC_000002.10:g.179209684G>T	NCBI36
NG_011618.3:g.199091C>A , LRG_391:g.199091C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33311C>A	ENSP00000343764.6:p.Ala11104Asp
ENST00000342175.11:c.14396C>A	ENSP00000340554.6:p.Ala4799Asp
ENST00000359218.10:c.14195C>A	ENSP00000352154.5:p.Ala4732Asp
ENST00000342175.10:c.14396C>A	ENSP00000340554.6:p.Ala4799Asp
ENST00000342992.10:c.33311C>A	ENSP00000343764.6:p.Ala11104Asp
ENST00000359218.9:c.14195C>A	ENSP00000352154.5:p.Ala4732Asp
ENST00000460472.6:c.13820C>A	ENSP00000434586.1:p.Ala4607Asp
ENST00000589042.5:c.41015C>A MANE Select	ENSP00000467141.1:p.Ala13672Asp
ENST00000591111.5:c.36092C>A	ENSP00000465570.1:p.Ala12031Asp
ENST00000615779.4:c.36092C>A	ENSP00000483597.1:p.Ala12031Asp
NM_001256850.1:c.36092C>A	NP_001243779.1:p.Ala12031Asp
NM_001267550.2:c.41015C>A MANE Select	NP_001254479.2:p.Ala13672Asp
NM_003319.4:c.13820C>A	NP_003310.4:p.Ala4607Asp
NM_133378.4:c.33311C>A	NP_596869.4:p.Ala11104Asp
NM_133432.3:c.14195C>A	NP_597676.3:p.Ala4732Asp
NM_133437.4:c.14396C>A	NP_597681.4:p.Ala4799Asp
XM_011511729.1:c.40112C>A	XP_011510031.1:p.Ala13371Asp
XM_011511730.1:c.14006C>A	XP_011510032.1:p.Ala4669Asp
XM_011511731.1:c.13865C>A	XP_011510033.1:p.Ala4622Asp
XM_017004819.1:c.39908C>A	XP_016860308.1:p.Ala13303Asp
XM_017004820.1:c.35306C>A	XP_016860309.1:p.Ala11769Asp
XM_017004821.1:c.35303C>A	XP_016860310.1:p.Ala11768Asp
XM_017004822.1:c.32345C>A	XP_016860311.1:p.Ala10782Asp
XM_017004823.1:c.13961C>A	XP_016860312.1:p.Ala4654Asp
XM_024453094.1:c.35456C>A	XP_024308862.1:p.Ala11819Asp
XM_024453095.1:c.35453C>A	XP_024308863.1:p.Ala11818Asp
XM_024453096.1:c.34886C>A	XP_024308864.1:p.Ala11629Asp
XM_024453097.1:c.32228C>A	XP_024308865.1:p.Ala10743Asp
XM_024453098.1:c.32147C>A	XP_024308866.1:p.Ala10716Asp
XM_024453099.1:c.13910C>A	XP_024308867.1:p.Ala4637Asp
XM_024453100.1:c.3764C>A	XP_024308868.1:p.Ala1255Asp