Canonical Allele Identifier: CA349417035

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.94958A>G (TTN)	ENSP00000343764.6:p.Tyr31653Cys
ENST00000342175.11:c.76043A>G (TTN)	ENSP00000340554.6:p.Tyr25348Cys
ENST00000359218.10:c.75842A>G (TTN)	ENSP00000352154.5:p.Tyr25281Cys
ENST00000342175.10:c.76043A>G (TTN)	ENSP00000340554.6:p.Tyr25348Cys
ENST00000342992.10:c.94958A>G (TTN)	ENSP00000343764.6:p.Tyr31653Cys
ENST00000359218.9:c.75842A>G (TTN)	ENSP00000352154.5:p.Tyr25281Cys
ENST00000460472.6:c.75467A>G (TTN)	ENSP00000434586.1:p.Tyr25156Cys
ENST00000589042.5:c.102662A>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr34221Cys
ENST00000591111.5:c.97739A>G (TTN)	ENSP00000465570.1:p.Tyr32580Cys
ENST00000615779.4:c.97739A>G (TTN)	ENSP00000483597.1:p.Tyr32580Cys
NM_001256850.1:c.97739A>G (TTN)	NP_001243779.1:p.Tyr32580Cys
NM_001267550.2:c.102662A>G (TTN) MANE Select	NP_001254479.2:p.Tyr34221Cys
NM_003319.4:c.75467A>G (TTN)	NP_003310.4:p.Tyr25156Cys
NM_133378.4:c.94958A>G (TTN)	NP_596869.4:p.Tyr31653Cys
NM_133432.3:c.75842A>G (TTN)	NP_597676.3:p.Tyr25281Cys
NM_133437.4:c.76043A>G (TTN)	NP_597681.4:p.Tyr25348Cys
NR_038271.1:n.446+10317T>C (TTN-AS1)
NR_038272.1:n.220-1779T>C (TTN-AS1)
XM_011511729.1:c.101759A>G (TTN)	XP_011510031.1:p.Tyr33920Cys
XM_011511730.1:c.75653A>G (TTN)	XP_011510032.1:p.Tyr25218Cys
XM_011511731.1:c.75512A>G (TTN)	XP_011510033.1:p.Tyr25171Cys
XM_017004819.1:c.101555A>G (TTN)	XP_016860308.1:p.Tyr33852Cys
XM_017004820.1:c.96953A>G (TTN)	XP_016860309.1:p.Tyr32318Cys
XM_017004821.1:c.96950A>G (TTN)	XP_016860310.1:p.Tyr32317Cys
XM_017004822.1:c.93992A>G (TTN)	XP_016860311.1:p.Tyr31331Cys
XM_017004823.1:c.75608A>G (TTN)	XP_016860312.1:p.Tyr25203Cys
XM_024453094.1:c.97103A>G (TTN)	XP_024308862.1:p.Tyr32368Cys
XM_024453095.1:c.97100A>G (TTN)	XP_024308863.1:p.Tyr32367Cys
XM_024453096.1:c.96533A>G (TTN)	XP_024308864.1:p.Tyr32178Cys
XM_024453097.1:c.93875A>G (TTN)	XP_024308865.1:p.Tyr31292Cys
XM_024453098.1:c.93794A>G (TTN)	XP_024308866.1:p.Tyr31265Cys
XM_024453099.1:c.75557A>G (TTN)	XP_024308867.1:p.Tyr25186Cys
XM_024453100.1:c.65411A>G (TTN)	XP_024308868.1:p.Tyr21804Cys