Canonical Allele Identifier: CA402156814

Gene: TTR

Linked Data

• ClinVar Variation Id: 576496
• ClinVar RCV Id: RCV000699004 ; RCV000714132
• dbSNP Id: rs1567945684
• gnomAD v4: 18-31592991-G-T
• MyVariant Identifiers: chr18:g.29172954G>T (hg19) ; chr18:g.31592991G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592991G>T , CM000680.2:g.31592991G>T	GRCh38
NC_000018.9:g.29172954G>T , CM000680.1:g.29172954G>T	GRCh37
NC_000018.8:g.27426952G>T	NCBI36
NG_009490.1:g.6225G>T , LRG_416:g.6225G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.165G>T MANE Select	ENSP00000237014.4:p.Lys55Asn
ENST00000610404.5:c.69G>T	ENSP00000477599.2:p.Lys23Asn
ENST00000649620.1:c.165G>T	ENSP00000497927.1:p.Lys55Asn
ENST00000237014.7:c.165G>T	ENSP00000237014.3:p.Lys55Asn
ENST00000432547.7:n.191G>T
ENST00000541025.2:n.191G>T
ENST00000610404.4:c.165G>T	ENSP00000477599.1:p.Lys55Asn
ENST00000613781.1:c.165G>T	ENSP00000479174.1:p.Lys55Asn
NM_000371.3:c.165G>T , LRG_416t1:c.165G>T	NP_000362.1:p.Lys55Asn
NM_000371.4:c.165G>T MANE Select	NP_000362.1:p.Lys55Asn