Canonical Allele Identifier: CA2293889313
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598546_31598550delinsATCTG , CM000680.2:g.31598546_31598550delinsATCTG GRCh38
NC_000018.9:g.29178509_29178513delinsATCTG , CM000680.1:g.29178509_29178513delinsATCTG GRCh37
NC_000018.8:g.27432507_27432511delinsATCTG NCBI36
NG_009490.1:g.11780_11784delinsATCTG , LRG_416:g.11780_11784delinsATCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-22_337-18delinsATCTG MANE Select ENSP00000237014.4:n.337-22_337-18delinsAT...
ENST00000610404.5:c.241-22_241-18delinsATCTG ENSP00000477599.2:n.241-22_241-18delinsAT...
ENST00000649620.1:c.337-22_337-18delinsATCTG ENSP00000497927.1:n.337-22_337-18delinsAT...
ENST00000237014.7:c.337-22_337-18delinsATCTG ENSP00000237014.3:n.337-22_337-18delinsAT...
ENST00000610404.4:c.451-22_451-18delinsATCTG ENSP00000477599.1:n.451-22_451-18delinsAT...
ENST00000613781.1:c.337-22_337-18delinsATCTG ENSP00000479174.1:n.337-22_337-18delinsAT...
NM_000371.3:c.337-22_337-18delinsATCTG , LRG_416t1:c.337-22_337-18delinsATCTG NP_000362.1:n.337-22_337-18delinsATCTG
NM_000371.4:c.337-22_337-18delinsATCTG MANE Select NP_000362.1:n.337-22_337-18delinsATCTG