Canonical Allele Identifier: CA3164759
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186596870C>T , CM000666.2:g.186596870C>T GRCh38
NC_000004.11:g.187518024C>T , CM000666.1:g.187518024C>T GRCh37
NC_000004.10:g.187755018C>T NCBI36
NG_046994.1:g.135046G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441802.7:c.12670G>A MANE Select ENSP00000406229.2:p.Ala4224Thr
ENST00000441802.6:c.12670G>A ENSP00000406229.2:p.Ala4224Thr
ENST00000500085.2:n.362G>A
ENST00000507105.1:c.302+164G>A
ENST00000614102.4:c.12676G>A ENSP00000479573.1:p.Ala4226Thr
NM_005245.3:c.12670G>A NP_005236.2:p.Ala4224Thr
XM_005262834.2:c.12670G>A XP_005262891.1:p.Ala4224Thr
XM_005262835.1:c.12670G>A XP_005262892.1:p.Ala4224Thr
XM_006714139.2:c.12670G>A XP_006714202.1:p.Ala4224Thr
XM_005262834.3:c.12670G>A XP_005262891.1:p.Ala4224Thr
XM_005262835.2:c.12670G>A XP_005262892.1:p.Ala4224Thr
XM_006714139.3:c.12670G>A XP_006714202.1:p.Ala4224Thr
NM_005245.4:c.12670G>A MANE Select NP_005236.2:p.Ala4224Thr