Canonical Allele Identifier: CA509459981
Gene: FERMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.6077549C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6096902C>T , CM000682.2:g.6096902C>T GRCh38
NC_000020.10:g.6077549C>T , CM000682.1:g.6077549C>T GRCh37
NC_000020.9:g.6025549C>T NCBI36
NG_016213.1:g.31643G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699095.1:c.1089G>A ENSP00000514127.1:p.Leu363=
ENST00000699096.1:n.1551G>A
ENST00000699097.1:n.259G>A
ENST00000217289.9:c.1089G>A MANE Select ENSP00000217289.4:p.Leu363=
ENST00000217289.8:c.1089G>A ENSP00000217289.4:p.Leu363=
ENST00000536936.1:c.318G>A ENSP00000441063.1:p.Leu106=
NM_017671.4:c.1089G>A NP_060141.3:p.Leu363=
XM_024451935.1:c.1089G>A XP_024307703.1:p.Leu363=
NM_017671.5:c.1089G>A MANE Select NP_060141.3:p.Leu363=
Search 100 bp 5'
Search 100 bp 3'