Canonical Allele Identifier: CA2293889389

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598677_31598686delinsGGACTTCTCC , CM000680.2:g.31598677_31598686delinsGGACTTCTCC	GRCh38
NC_000018.9:g.29178640_29178649delinsGGACTTCTCC , CM000680.1:g.29178640_29178649delinsGGACTTCTCC	GRCh37
NC_000018.8:g.27432638_27432647delinsGGACTTCTCC	NCBI36
NG_009490.1:g.11911_11920delinsGGACTTCTCC , LRG_416:g.11911_11920delinsGGACTTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.*2_*11delinsGGACTTCTCC MANE Select	ENSP00000237014.4:n.*2_*11delinsGGACTTCTCC
ENST00000610404.5:c.*2_*11delinsGGACTTCTCC	ENSP00000477599.2:n.*2_*11delinsGGACTTCTCC
ENST00000649620.1:c.*2_*11delinsGGACTTCTCC	ENSP00000497927.1:n.*2_*11delinsGGACTTCTCC
ENST00000237014.7:c.*2_*11delinsGGACTTCTCC	ENSP00000237014.3:n.*2_*11delinsGGACTTCTCC
ENST00000610404.4:c.*2_*11delinsGGACTTCTCC	ENSP00000477599.1:n.*2_*11delinsGGACTTCTCC
NM_000371.3:c.*2_*11delinsGGACTTCTCC , LRG_416t1:c.*2_*11delinsGGACTTCTCC	NP_000362.1:n.*2_*11delinsGGACTTCTCC
NM_000371.4:c.*2_*11delinsGGACTTCTCC MANE Select	NP_000362.1:n.*2_*11delinsGGACTTCTCC