Canonical Allele Identifier: CA402156517

Gene: TTR

Linked Data

• ClinVar Variation Id: 1502316
• ClinVar RCV Id: RCV002020174
• dbSNP Id: rs2144406521
• MyVariant Identifiers: chr18:g.29172880C>T (hg19) ; chr18:g.31592917C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592917C>T , CM000680.2:g.31592917C>T	GRCh38
NC_000018.9:g.29172880C>T , CM000680.1:g.29172880C>T	GRCh37
NC_000018.8:g.27426878C>T	NCBI36
NG_009490.1:g.6151C>T , LRG_416:g.6151C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.91C>T MANE Select	ENSP00000237014.4:p.Pro31Ser
ENST00000610404.5:c.-6C>T	ENSP00000477599.2:n.-6C>T
ENST00000649620.1:c.91C>T	ENSP00000497927.1:p.Pro31Ser
ENST00000237014.7:c.91C>T	ENSP00000237014.3:p.Pro31Ser
ENST00000432547.7:n.117C>T
ENST00000541025.2:n.117C>T
ENST00000610404.4:c.91C>T	ENSP00000477599.1:p.Pro31Ser
ENST00000613781.1:c.91C>T	ENSP00000479174.1:p.Pro31Ser
NM_000371.3:c.91C>T , LRG_416t1:c.91C>T	NP_000362.1:p.Pro31Ser
NM_000371.4:c.91C>T MANE Select	NP_000362.1:p.Pro31Ser