Canonical Allele Identifier: CA1520094218
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186603780G= , CM000666.2:g.186603780G= GRCh38
NC_000004.11:g.187524934G= , CM000666.1:g.187524934G= GRCh37
NC_000004.10:g.187761928G= NCBI36
NG_046994.1:g.128136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000441802.7:c.10746C= MANE Select ENSP00000406229.2:p.Leu3582=
ENST00000441802.6:c.10746C= ENSP00000406229.2:p.Leu3582=
ENST00000614102.4:c.10752C= ENSP00000479573.1:p.Leu3584=
NM_005245.3:c.10746C= NP_005236.2:p.Leu3582=
XM_005262834.2:c.10746C= XP_005262891.1:p.Leu3582=
XM_005262835.1:c.10746C= XP_005262892.1:p.Leu3582=
XM_006714139.2:c.10746C= XP_006714202.1:p.Leu3582=
XM_005262834.3:c.10746C= XP_005262891.1:p.Leu3582=
XM_005262835.2:c.10746C= XP_005262892.1:p.Leu3582=
XM_006714139.3:c.10746C= XP_006714202.1:p.Leu3582=
NM_005245.4:c.10746C= MANE Select NP_005236.2:p.Leu3582=