Canonical Allele Identifier: CA349417036

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179398680T>G (hg19) ; chr2:g.178533953T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178533953T>G , CM000664.2:g.178533953T>G	GRCh38
NC_000002.11:g.179398680T>G , CM000664.1:g.179398680T>G	GRCh37
NC_000002.10:g.179106926T>G	NCBI36
NG_011618.3:g.301850A>C , LRG_391:g.301850A>C
NG_051363.1:g.16127T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.94958A>C (TTN)	ENSP00000343764.6:p.Tyr31653Ser
ENST00000342175.11:c.76043A>C (TTN)	ENSP00000340554.6:p.Tyr25348Ser
ENST00000359218.10:c.75842A>C (TTN)	ENSP00000352154.5:p.Tyr25281Ser
ENST00000342175.10:c.76043A>C (TTN)	ENSP00000340554.6:p.Tyr25348Ser
ENST00000342992.10:c.94958A>C (TTN)	ENSP00000343764.6:p.Tyr31653Ser
ENST00000359218.9:c.75842A>C (TTN)	ENSP00000352154.5:p.Tyr25281Ser
ENST00000460472.6:c.75467A>C (TTN)	ENSP00000434586.1:p.Tyr25156Ser
ENST00000589042.5:c.102662A>C (TTN) MANE Select	ENSP00000467141.1:p.Tyr34221Ser
ENST00000591111.5:c.97739A>C (TTN)	ENSP00000465570.1:p.Tyr32580Ser
ENST00000615779.4:c.97739A>C (TTN)	ENSP00000483597.1:p.Tyr32580Ser
NM_001256850.1:c.97739A>C (TTN)	NP_001243779.1:p.Tyr32580Ser
NM_001267550.2:c.102662A>C (TTN) MANE Select	NP_001254479.2:p.Tyr34221Ser
NM_003319.4:c.75467A>C (TTN)	NP_003310.4:p.Tyr25156Ser
NM_133378.4:c.94958A>C (TTN)	NP_596869.4:p.Tyr31653Ser
NM_133432.3:c.75842A>C (TTN)	NP_597676.3:p.Tyr25281Ser
NM_133437.4:c.76043A>C (TTN)	NP_597681.4:p.Tyr25348Ser
NR_038271.1:n.446+10317T>G (TTN-AS1)
NR_038272.1:n.220-1779T>G (TTN-AS1)
XM_011511729.1:c.101759A>C (TTN)	XP_011510031.1:p.Tyr33920Ser
XM_011511730.1:c.75653A>C (TTN)	XP_011510032.1:p.Tyr25218Ser
XM_011511731.1:c.75512A>C (TTN)	XP_011510033.1:p.Tyr25171Ser
XM_017004819.1:c.101555A>C (TTN)	XP_016860308.1:p.Tyr33852Ser
XM_017004820.1:c.96953A>C (TTN)	XP_016860309.1:p.Tyr32318Ser
XM_017004821.1:c.96950A>C (TTN)	XP_016860310.1:p.Tyr32317Ser
XM_017004822.1:c.93992A>C (TTN)	XP_016860311.1:p.Tyr31331Ser
XM_017004823.1:c.75608A>C (TTN)	XP_016860312.1:p.Tyr25203Ser
XM_024453094.1:c.97103A>C (TTN)	XP_024308862.1:p.Tyr32368Ser
XM_024453095.1:c.97100A>C (TTN)	XP_024308863.1:p.Tyr32367Ser
XM_024453096.1:c.96533A>C (TTN)	XP_024308864.1:p.Tyr32178Ser
XM_024453097.1:c.93875A>C (TTN)	XP_024308865.1:p.Tyr31292Ser
XM_024453098.1:c.93794A>C (TTN)	XP_024308866.1:p.Tyr31265Ser
XM_024453099.1:c.75557A>C (TTN)	XP_024308867.1:p.Tyr25186Ser
XM_024453100.1:c.65411A>C (TTN)	XP_024308868.1:p.Tyr21804Ser