Canonical Allele Identifier: CA1520094216
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186603769A= , CM000666.2:g.186603769A= GRCh38
NC_000004.11:g.187524923A= , CM000666.1:g.187524923A= GRCh37
NC_000004.10:g.187761917A= NCBI36
NG_046994.1:g.128147T=

Transcript Alleles

HGVS Amino-acid change
ENST00000441802.7:c.10757T= MANE Select ENSP00000406229.2:p.Met3586=
ENST00000441802.6:c.10757T= ENSP00000406229.2:p.Met3586=
ENST00000614102.4:c.10763T= ENSP00000479573.1:p.Met3588=
NM_005245.3:c.10757T= NP_005236.2:p.Met3586=
XM_005262834.2:c.10757T= XP_005262891.1:p.Met3586=
XM_005262835.1:c.10757T= XP_005262892.1:p.Met3586=
XM_006714139.2:c.10757T= XP_006714202.1:p.Met3586=
XM_005262834.3:c.10757T= XP_005262891.1:p.Met3586=
XM_005262835.2:c.10757T= XP_005262892.1:p.Met3586=
XM_006714139.3:c.10757T= XP_006714202.1:p.Met3586=
NM_005245.4:c.10757T= MANE Select NP_005236.2:p.Met3586=