Canonical Allele Identifier: CA2293887935

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595429_31595433delinsATTTC , CM000680.2:g.31595429_31595433delinsATTTC	GRCh38
NC_000018.9:g.29175392_29175396delinsATTTC , CM000680.1:g.29175392_29175396delinsATTTC	GRCh37
NC_000018.8:g.27429390_27429394delinsATTTC	NCBI36
NG_009490.1:g.8663_8667delinsATTTC , LRG_416:g.8663_8667delinsATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+174_336+178delinsATTTC MANE Select	ENSP00000237014.4:n.336+174_336+178delinsATTTC
ENST00000610404.5:c.240+174_240+178delinsATTTC	ENSP00000477599.2:n.240+174_240+178delinsATTTC
ENST00000649620.1:c.336+174_336+178delinsATTTC	ENSP00000497927.1:n.336+174_336+178delinsATTTC
ENST00000237014.7:c.336+174_336+178delinsATTTC	ENSP00000237014.3:n.336+174_336+178delinsATTTC
ENST00000541025.2:n.536_540delinsATTTC
ENST00000610404.4:c.357+153_357+157delinsATTTC	ENSP00000477599.1:n.357+153_357+157delinsATTTC
ENST00000613781.1:c.336+174_336+178delinsATTTC	ENSP00000479174.1:n.336+174_336+178delinsATTTC
NM_000371.3:c.336+174_336+178delinsATTTC , LRG_416t1:c.336+174_336+178delinsATTTC	NP_000362.1:n.336+174_336+178delinsATTTC
NM_000371.4:c.336+174_336+178delinsATTTC MANE Select	NP_000362.1:n.336+174_336+178delinsATTTC