Canonical Allele Identifier: CA402157065
Gene: TTR HGNC NCBI

Linked Data

dbSNP Id: rs1197116703

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31595207A>T , CM000680.2:g.31595207A>T GRCh38
NC_000018.9:g.29175170A>T , CM000680.1:g.29175170A>T GRCh37
NC_000018.8:g.27429168A>T NCBI36
NG_009490.1:g.8441A>T , LRG_416:g.8441A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.288A>T MANE Select ENSP00000237014.4:p.Lys96Asn
ENST00000610404.5:c.192A>T ENSP00000477599.2:p.Lys64Asn
ENST00000649620.1:c.288A>T ENSP00000497927.1:p.Lys96Asn
ENST00000237014.7:c.288A>T ENSP00000237014.3:p.Lys96Asn
ENST00000541025.2:n.314A>T
ENST00000610404.4:c.288A>T ENSP00000477599.1:p.Lys96Asn
ENST00000613781.1:c.288A>T ENSP00000479174.1:p.Lys96Asn
NM_000371.3:c.288A>T , LRG_416t1:c.288A>T NP_000362.1:p.Lys96Asn
NM_000371.4:c.288A>T MANE Select NP_000362.1:p.Lys96Asn