Canonical Allele Identifier: CA1520094250
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186603866A= , CM000666.2:g.186603866A= GRCh38
NC_000004.11:g.187525020A= , CM000666.1:g.187525020A= GRCh37
NC_000004.10:g.187762014A= NCBI36
NG_046994.1:g.128050T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441802.7:c.10660T= MANE Select ENSP00000406229.2:p.Ser3554=
ENST00000441802.6:c.10660T= ENSP00000406229.2:p.Ser3554=
ENST00000614102.4:c.10666T= ENSP00000479573.1:p.Ser3556=
NM_005245.3:c.10660T= NP_005236.2:p.Ser3554=
XM_005262834.2:c.10660T= XP_005262891.1:p.Ser3554=
XM_005262835.1:c.10660T= XP_005262892.1:p.Ser3554=
XM_006714139.2:c.10660T= XP_006714202.1:p.Ser3554=
XM_005262834.3:c.10660T= XP_005262891.1:p.Ser3554=
XM_005262835.2:c.10660T= XP_005262892.1:p.Ser3554=
XM_006714139.3:c.10660T= XP_006714202.1:p.Ser3554=
NM_005245.4:c.10660T= MANE Select NP_005236.2:p.Ser3554=