Canonical Allele Identifier: CA3164863
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186597747G>A , CM000666.2:g.186597747G>A GRCh38
NC_000004.11:g.187518901G>A , CM000666.1:g.187518901G>A GRCh37
NC_000004.10:g.187755895G>A NCBI36
NG_046994.1:g.134169C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441802.7:c.12303C>T MANE Select ENSP00000406229.2:p.Gly4101=
ENST00000441802.6:c.12303C>T ENSP00000406229.2:p.Gly4101=
ENST00000507105.1:c.99C>T
ENST00000507662.1:n.202C>T
ENST00000512347.1:n.495C>T
ENST00000614102.4:c.12309C>T ENSP00000479573.1:p.Gly4103=
NM_005245.3:c.12303C>T NP_005236.2:p.Gly4101=
XM_005262834.2:c.12303C>T XP_005262891.1:p.Gly4101=
XM_005262835.1:c.12303C>T XP_005262892.1:p.Gly4101=
XM_006714139.2:c.12303C>T XP_006714202.1:p.Gly4101=
XM_005262834.3:c.12303C>T XP_005262891.1:p.Gly4101=
XM_005262835.2:c.12303C>T XP_005262892.1:p.Gly4101=
XM_006714139.3:c.12303C>T XP_006714202.1:p.Gly4101=
NM_005245.4:c.12303C>T MANE Select NP_005236.2:p.Gly4101=