Canonical Allele Identifier: CA2293889373
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598651_31598654delinsTGTC , CM000680.2:g.31598651_31598654delinsTGTC GRCh38
NC_000018.9:g.29178614_29178617delinsTGTC , CM000680.1:g.29178614_29178617delinsTGTC GRCh37
NC_000018.8:g.27432612_27432615delinsTGTC NCBI36
NG_009490.1:g.11885_11888delinsTGTC , LRG_416:g.11885_11888delinsTGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.420_423delinsTGTC MANE Select ENSP00000237014.4:p.Ala140=
ENST00000610404.5:c.324_327delinsTGTC ENSP00000477599.2:p.Ala108=
ENST00000649620.1:c.420_423delinsTGTC ENSP00000497927.1:p.Ala140=
ENST00000237014.7:c.420_423delinsTGTC ENSP00000237014.3:p.Ala140=
ENST00000610404.4:c.534_537delinsTGTC ENSP00000477599.1:p.Ala178=
ENST00000613781.1:c.396_399delinsTGTC ENSP00000479174.1:p.Ala132=
NM_000371.3:c.420_423delinsTGTC , LRG_416t1:c.420_423delinsTGTC NP_000362.1:p.Ala140=
NM_000371.4:c.420_423delinsTGTC MANE Select NP_000362.1:p.Ala140=