Canonical Allele Identifier: CA2641409535

Gene: TTR

Linked Data

• gnomAD v4: 18-31595330-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595330A>C , CM000680.2:g.31595330A>C	GRCh38
NC_000018.9:g.29175293A>C , CM000680.1:g.29175293A>C	GRCh37
NC_000018.8:g.27429291A>C	NCBI36
NG_009490.1:g.8564A>C , LRG_416:g.8564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+75A>C MANE Select	ENSP00000237014.4:n.336+75A>C
ENST00000610404.5:c.240+75A>C	ENSP00000477599.2:n.240+75A>C
ENST00000649620.1:c.336+75A>C	ENSP00000497927.1:n.336+75A>C
ENST00000237014.7:c.336+75A>C	ENSP00000237014.3:n.336+75A>C
ENST00000541025.2:n.437A>C
ENST00000610404.4:c.357+54A>C	ENSP00000477599.1:n.357+54A>C
ENST00000613781.1:c.336+75A>C	ENSP00000479174.1:n.336+75A>C
NM_000371.3:c.336+75A>C , LRG_416t1:c.336+75A>C	NP_000362.1:n.336+75A>C
NM_000371.4:c.336+75A>C MANE Select	NP_000362.1:n.336+75A>C