Canonical Allele Identifier: CA349411922

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396986A>T (hg19) ; chr2:g.178532259A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532259A>T , CM000664.2:g.178532259A>T	GRCh38
NC_000002.11:g.179396986A>T , CM000664.1:g.179396986A>T	GRCh37
NC_000002.10:g.179105232A>T	NCBI36
NG_011618.3:g.303544T>A , LRG_391:g.303544T>A
NG_051363.1:g.14433A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96652T>A (TTN)	ENSP00000343764.6:p.Tyr32218Asn
ENST00000342175.11:c.77737T>A (TTN)	ENSP00000340554.6:p.Tyr25913Asn
ENST00000359218.10:c.77536T>A (TTN)	ENSP00000352154.5:p.Tyr25846Asn
ENST00000342175.10:c.77737T>A (TTN)	ENSP00000340554.6:p.Tyr25913Asn
ENST00000342992.10:c.96652T>A (TTN)	ENSP00000343764.6:p.Tyr32218Asn
ENST00000359218.9:c.77536T>A (TTN)	ENSP00000352154.5:p.Tyr25846Asn
ENST00000460472.6:c.77161T>A (TTN)	ENSP00000434586.1:p.Tyr25721Asn
ENST00000589042.5:c.104356T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr34786Asn
ENST00000591111.5:c.99433T>A (TTN)	ENSP00000465570.1:p.Tyr33145Asn
ENST00000615779.4:c.99433T>A (TTN)	ENSP00000483597.1:p.Tyr33145Asn
NM_001256850.1:c.99433T>A (TTN)	NP_001243779.1:p.Tyr33145Asn
NM_001267550.2:c.104356T>A (TTN) MANE Select	NP_001254479.2:p.Tyr34786Asn
NM_003319.4:c.77161T>A (TTN)	NP_003310.4:p.Tyr25721Asn
NM_133378.4:c.96652T>A (TTN)	NP_596869.4:p.Tyr32218Asn
NM_133432.3:c.77536T>A (TTN)	NP_597676.3:p.Tyr25846Asn
NM_133437.4:c.77737T>A (TTN)	NP_597681.4:p.Tyr25913Asn
NR_038271.1:n.446+8623A>T (TTN-AS1)
NR_038272.1:n.220-3473A>T (TTN-AS1)
XM_011511729.1:c.103453T>A (TTN)	XP_011510031.1:p.Tyr34485Asn
XM_011511730.1:c.77347T>A (TTN)	XP_011510032.1:p.Tyr25783Asn
XM_011511731.1:c.77206T>A (TTN)	XP_011510033.1:p.Tyr25736Asn
XM_017004819.1:c.103249T>A (TTN)	XP_016860308.1:p.Tyr34417Asn
XM_017004820.1:c.98647T>A (TTN)	XP_016860309.1:p.Tyr32883Asn
XM_017004821.1:c.98644T>A (TTN)	XP_016860310.1:p.Tyr32882Asn
XM_017004822.1:c.95686T>A (TTN)	XP_016860311.1:p.Tyr31896Asn
XM_017004823.1:c.77302T>A (TTN)	XP_016860312.1:p.Tyr25768Asn
XM_024453094.1:c.98797T>A (TTN)	XP_024308862.1:p.Tyr32933Asn
XM_024453095.1:c.98794T>A (TTN)	XP_024308863.1:p.Tyr32932Asn
XM_024453096.1:c.98227T>A (TTN)	XP_024308864.1:p.Tyr32743Asn
XM_024453097.1:c.95569T>A (TTN)	XP_024308865.1:p.Tyr31857Asn
XM_024453098.1:c.95488T>A (TTN)	XP_024308866.1:p.Tyr31830Asn
XM_024453099.1:c.77251T>A (TTN)	XP_024308867.1:p.Tyr25751Asn
XM_024453100.1:c.67105T>A (TTN)	XP_024308868.1:p.Tyr22369Asn