Canonical Allele Identifier: CA408176203
Gene: FERMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.6060109A>T (hg19) chr20:g.6079462A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6079462A>T , CM000682.2:g.6079462A>T GRCh38
NC_000020.10:g.6060109A>T , CM000682.1:g.6060109A>T GRCh37
NC_000020.9:g.6008109A>T NCBI36
NG_016213.1:g.49083T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699095.1:c.1834T>A ENSP00000514127.1:p.Trp612Arg
ENST00000217289.9:c.1834T>A MANE Select ENSP00000217289.4:p.Trp612Arg
ENST00000217289.8:c.1834T>A ENSP00000217289.4:p.Trp612Arg
ENST00000478194.1:n.794T>A
ENST00000536936.1:c.1063T>A ENSP00000441063.1:p.Trp355Arg
NM_017671.4:c.1834T>A NP_060141.3:p.Trp612Arg
XM_024451935.1:c.1834T>A XP_024307703.1:p.Trp612Arg
NM_017671.5:c.1834T>A MANE Select NP_060141.3:p.Trp612Arg
Search 100 bp 5'
Search 100 bp 3'