Canonical Allele Identifier: CA2293887891

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595320_31595322delinsGCA , CM000680.2:g.31595320_31595322delinsGCA	GRCh38
NC_000018.9:g.29175283_29175285delinsGCA , CM000680.1:g.29175283_29175285delinsGCA	GRCh37
NC_000018.8:g.27429281_27429283delinsGCA	NCBI36
NG_009490.1:g.8554_8556delinsGCA , LRG_416:g.8554_8556delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+65_336+67delinsGCA MANE Select	ENSP00000237014.4:n.336+65_336+67delinsGCA
ENST00000610404.5:c.240+65_240+67delinsGCA	ENSP00000477599.2:n.240+65_240+67delinsGCA
ENST00000649620.1:c.336+65_336+67delinsGCA	ENSP00000497927.1:n.336+65_336+67delinsGCA
ENST00000237014.7:c.336+65_336+67delinsGCA	ENSP00000237014.3:n.336+65_336+67delinsGCA
ENST00000541025.2:n.427_429delinsGCA
ENST00000610404.4:c.357+44_357+46delinsGCA	ENSP00000477599.1:n.357+44_357+46delinsGCA
ENST00000613781.1:c.336+65_336+67delinsGCA	ENSP00000479174.1:n.336+65_336+67delinsGCA
NM_000371.3:c.336+65_336+67delinsGCA , LRG_416t1:c.336+65_336+67delinsGCA	NP_000362.1:n.336+65_336+67delinsGCA
NM_000371.4:c.336+65_336+67delinsGCA MANE Select	NP_000362.1:n.336+65_336+67delinsGCA