Canonical Allele Identifier: CA2641410494

Gene: TTR

Linked Data

• gnomAD v4: 18-31598521-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598525_31598526dup , CM000680.2:g.31598525_31598526dup	GRCh38
NC_000018.9:g.29178488_29178489dup , CM000680.1:g.29178488_29178489dup	GRCh37
NC_000018.8:g.27432486_27432487dup	NCBI36
NG_009490.1:g.11759_11760dup , LRG_416:g.11759_11760dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.337-43_337-42dup MANE Select	ENSP00000237014.4:n.337-43_337-42dup
ENST00000610404.5:c.241-43_241-42dup	ENSP00000477599.2:n.241-43_241-42dup
ENST00000649620.1:c.337-43_337-42dup	ENSP00000497927.1:n.337-43_337-42dup
ENST00000237014.7:c.337-43_337-42dup	ENSP00000237014.3:n.337-43_337-42dup
ENST00000610404.4:c.451-43_451-42dup	ENSP00000477599.1:n.451-43_451-42dup
ENST00000613781.1:c.337-43_337-42dup	ENSP00000479174.1:n.337-43_337-42dup
NM_000371.3:c.337-43_337-42dup , LRG_416t1:c.337-43_337-42dup	NP_000362.1:n.337-43_337-42dup
NM_000371.4:c.337-43_337-42dup MANE Select	NP_000362.1:n.337-43_337-42dup