Canonical Allele Identifier: CA538438050

Gene: TTN

Linked Data

• dbSNP Id: rs1429684879
• gnomAD v2: 2-179615286-A-G
• MyVariant Identifiers: chr2:g.179615286A>G (hg19) ; chr2:g.178750559A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178750559A>G , CM000664.2:g.178750559A>G	GRCh38
NC_000002.11:g.179615286A>G , CM000664.1:g.179615286A>G	GRCh37
NC_000002.10:g.179323531A>G	NCBI36
NG_011618.3:g.85244T>C , LRG_391:g.85244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.10360+2565T>C	ENSP00000343764.6:n.10360+2565T>C
ENST00000342175.11:c.10798+2565T>C	ENSP00000340554.6:n.10798+2565T>C
ENST00000359218.10:c.10597+2565T>C	ENSP00000352154.5:n.10597+2565T>C
ENST00000360870.10:c.11841T>C MANE Plus Clinical	ENSP00000354117.4:p.Leu3947=
ENST00000342175.10:c.10798+2565T>C	ENSP00000340554.6:n.10798+2565T>C
ENST00000342992.10:c.10360+2565T>C	ENSP00000343764.6:n.10360+2565T>C
ENST00000359218.9:c.10597+2565T>C	ENSP00000352154.5:n.10597+2565T>C
ENST00000360870.9:c.11841T>C	ENSP00000354117.4:p.Leu3947=
ENST00000460472.6:c.10222+2565T>C	ENSP00000434586.1:n.10222+2565T>C
ENST00000589042.5:c.11311+2565T>C MANE Select	ENSP00000467141.1:n.11311+2565T>C
ENST00000591111.5:c.10360+2565T>C	ENSP00000465570.1:n.10360+2565T>C
ENST00000615779.4:c.10360+2565T>C	ENSP00000483597.1:n.10360+2565T>C
NM_001256850.1:c.10360+2565T>C	NP_001243779.1:n.10360+2565T>C
NM_001267550.2:c.11311+2565T>C MANE Select	NP_001254479.2:n.11311+2565T>C
NM_003319.4:c.10222+2565T>C	NP_003310.4:n.10222+2565T>C
NM_133378.4:c.10360+2565T>C	NP_596869.4:n.10360+2565T>C
NM_133379.4:c.11841T>C , LRG_391t2:c.11841T>C	NP_596870.2:p.Leu3947=
NM_133432.3:c.10597+2565T>C	NP_597676.3:n.10597+2565T>C
NM_133437.4:c.10798+2565T>C	NP_597681.4:n.10798+2565T>C
XM_011511729.1:c.10408+2565T>C	XP_011510031.1:n.10408+2565T>C
XM_011511730.1:c.10408+2565T>C	XP_011510032.1:n.10408+2565T>C
XM_011511731.1:c.10267+2565T>C	XP_011510033.1:n.10267+2565T>C
XM_011511732.1:c.11886T>C	XP_011510034.1:p.Leu3962=
XM_017004819.1:c.10363+2565T>C	XP_016860308.1:n.10363+2565T>C
XM_017004820.1:c.10363+2565T>C	XP_016860309.1:n.10363+2565T>C
XM_017004821.1:c.10360+2565T>C	XP_016860310.1:n.10360+2565T>C
XM_017004822.1:c.10363+2565T>C	XP_016860311.1:n.10363+2565T>C
XM_017004823.1:c.10363+2565T>C	XP_016860312.1:n.10363+2565T>C
XM_024453094.1:c.10363+2565T>C	XP_024308862.1:n.10363+2565T>C
XM_024453095.1:c.10363+2565T>C	XP_024308863.1:n.10363+2565T>C
XM_024453096.1:c.10363+2565T>C	XP_024308864.1:n.10363+2565T>C
XM_024453097.1:c.10363+2565T>C	XP_024308865.1:n.10363+2565T>C
XM_024453098.1:c.10363+2565T>C	XP_024308866.1:n.10363+2565T>C
XM_024453099.1:c.10363+2565T>C	XP_024308867.1:n.10363+2565T>C
NM_133379.5:c.11841T>C MANE Plus Clinical	NP_596870.2:p.Leu3947=