Canonical Allele Identifier: CA349455606

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408991T>C (hg19) ; chr2:g.178544264T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544264T>C , CM000664.2:g.178544264T>C	GRCh38
NC_000002.11:g.179408991T>C , CM000664.1:g.179408991T>C	GRCh37
NC_000002.10:g.179117237T>C	NCBI36
NG_011618.3:g.291539A>G , LRG_391:g.291539A>G
NG_051363.1:g.26438T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88261A>G (TTN)	ENSP00000343764.6:p.Asn29421Asp
ENST00000342175.11:c.69346A>G (TTN)	ENSP00000340554.6:p.Asn23116Asp
ENST00000359218.10:c.69145A>G (TTN)	ENSP00000352154.5:p.Asn23049Asp
ENST00000342175.10:c.69346A>G (TTN)	ENSP00000340554.6:p.Asn23116Asp
ENST00000342992.10:c.88261A>G (TTN)	ENSP00000343764.6:p.Asn29421Asp
ENST00000359218.9:c.69145A>G (TTN)	ENSP00000352154.5:p.Asn23049Asp
ENST00000460472.6:c.68770A>G (TTN)	ENSP00000434586.1:p.Asn22924Asp
ENST00000589042.5:c.95965A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn31989Asp
ENST00000591111.5:c.91042A>G (TTN)	ENSP00000465570.1:p.Asn30348Asp
ENST00000615779.4:c.91042A>G (TTN)	ENSP00000483597.1:p.Asn30348Asp
NM_001256850.1:c.91042A>G (TTN)	NP_001243779.1:p.Asn30348Asp
NM_001267550.2:c.95965A>G (TTN) MANE Select	NP_001254479.2:p.Asn31989Asp
NM_003319.4:c.68770A>G (TTN)	NP_003310.4:p.Asn22924Asp
NM_133378.4:c.88261A>G (TTN)	NP_596869.4:p.Asn29421Asp
NM_133432.3:c.69145A>G (TTN)	NP_597676.3:p.Asn23049Asp
NM_133437.4:c.69346A>G (TTN)	NP_597681.4:p.Asn23116Asp
NR_038271.1:n.446+20628T>C (TTN-AS1)
NR_038272.1:n.2043+1903T>C (TTN-AS1)
XM_011511729.1:c.95062A>G (TTN)	XP_011510031.1:p.Asn31688Asp
XM_011511730.1:c.68956A>G (TTN)	XP_011510032.1:p.Asn22986Asp
XM_011511731.1:c.68815A>G (TTN)	XP_011510033.1:p.Asn22939Asp
XM_017004819.1:c.94858A>G (TTN)	XP_016860308.1:p.Asn31620Asp
XM_017004820.1:c.90256A>G (TTN)	XP_016860309.1:p.Asn30086Asp
XM_017004821.1:c.90253A>G (TTN)	XP_016860310.1:p.Asn30085Asp
XM_017004822.1:c.87295A>G (TTN)	XP_016860311.1:p.Asn29099Asp
XM_017004823.1:c.68911A>G (TTN)	XP_016860312.1:p.Asn22971Asp
XM_024453094.1:c.90406A>G (TTN)	XP_024308862.1:p.Asn30136Asp
XM_024453095.1:c.90403A>G (TTN)	XP_024308863.1:p.Asn30135Asp
XM_024453096.1:c.89836A>G (TTN)	XP_024308864.1:p.Asn29946Asp
XM_024453097.1:c.87178A>G (TTN)	XP_024308865.1:p.Asn29060Asp
XM_024453098.1:c.87097A>G (TTN)	XP_024308866.1:p.Asn29033Asp
XM_024453099.1:c.68860A>G (TTN)	XP_024308867.1:p.Asn22954Asp
XM_024453100.1:c.58714A>G (TTN)	XP_024308868.1:p.Asn19572Asp