Canonical Allele Identifier: CA2293887933

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595425_31595427delinsGCA , CM000680.2:g.31595425_31595427delinsGCA	GRCh38
NC_000018.9:g.29175388_29175390delinsGCA , CM000680.1:g.29175388_29175390delinsGCA	GRCh37
NC_000018.8:g.27429386_27429388delinsGCA	NCBI36
NG_009490.1:g.8659_8661delinsGCA , LRG_416:g.8659_8661delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+170_336+172delinsGCA MANE Select	ENSP00000237014.4:n.336+170_336+172delinsGCA
ENST00000610404.5:c.240+170_240+172delinsGCA	ENSP00000477599.2:n.240+170_240+172delinsGCA
ENST00000649620.1:c.336+170_336+172delinsGCA	ENSP00000497927.1:n.336+170_336+172delinsGCA
ENST00000237014.7:c.336+170_336+172delinsGCA	ENSP00000237014.3:n.336+170_336+172delinsGCA
ENST00000541025.2:n.532_534delinsGCA
ENST00000610404.4:c.357+149_357+151delinsGCA	ENSP00000477599.1:n.357+149_357+151delinsGCA
ENST00000613781.1:c.336+170_336+172delinsGCA	ENSP00000479174.1:n.336+170_336+172delinsGCA
NM_000371.3:c.336+170_336+172delinsGCA , LRG_416t1:c.336+170_336+172delinsGCA	NP_000362.1:n.336+170_336+172delinsGCA
NM_000371.4:c.336+170_336+172delinsGCA MANE Select	NP_000362.1:n.336+170_336+172delinsGCA