Canonical Allele Identifier: CA2347801831
Gene: FERMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6096910T= , CM000682.2:g.6096910T= GRCh38
NC_000020.10:g.6077557T= , CM000682.1:g.6077557T= GRCh37
NC_000020.9:g.6025557T= NCBI36
NG_016213.1:g.31635A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699095.1:c.1081A= ENSP00000514127.1:p.Ser361=
ENST00000699096.1:n.1543A=
ENST00000699097.1:n.251A=
ENST00000217289.9:c.1081A= MANE Select ENSP00000217289.4:p.Ser361=
ENST00000217289.8:c.1081A= ENSP00000217289.4:p.Ser361=
ENST00000536936.1:c.310A= ENSP00000441063.1:p.Ser104=
NM_017671.4:c.1081A= NP_060141.3:p.Ser361=
XM_024451935.1:c.1081A= XP_024307703.1:p.Ser361=
NM_017671.5:c.1081A= MANE Select NP_060141.3:p.Ser361=