Canonical Allele Identifier: CA408182133
Gene: FERMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6096903A>T , CM000682.2:g.6096903A>T GRCh38
NC_000020.10:g.6077550A>T , CM000682.1:g.6077550A>T GRCh37
NC_000020.9:g.6025550A>T NCBI36
NG_016213.1:g.31642T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699095.1:c.1088T>A ENSP00000514127.1:p.Leu363Ter
ENST00000699096.1:n.1550T>A
ENST00000699097.1:n.258T>A
ENST00000217289.9:c.1088T>A MANE Select ENSP00000217289.4:p.Leu363Ter
ENST00000217289.8:c.1088T>A ENSP00000217289.4:p.Leu363Ter
ENST00000536936.1:c.317T>A ENSP00000441063.1:p.Leu106Ter
NM_017671.4:c.1088T>A NP_060141.3:p.Leu363Ter
XM_024451935.1:c.1088T>A XP_024307703.1:p.Leu363Ter
NM_017671.5:c.1088T>A MANE Select NP_060141.3:p.Leu363Ter