Canonical Allele Identifier: CA3164779
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186596970T>C , CM000666.2:g.186596970T>C GRCh38
NC_000004.11:g.187518124T>C , CM000666.1:g.187518124T>C GRCh37
NC_000004.10:g.187755118T>C NCBI36
NG_046994.1:g.134946A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000441802.7:c.12570A>G MANE Select ENSP00000406229.2:p.Ala4190=
ENST00000441802.6:c.12570A>G ENSP00000406229.2:p.Ala4190=
ENST00000500085.2:n.262A>G
ENST00000507105.1:c.302+64A>G
ENST00000614102.4:c.12576A>G ENSP00000479573.1:p.Ala4192=
NM_005245.3:c.12570A>G NP_005236.2:p.Ala4190=
XM_005262834.2:c.12570A>G XP_005262891.1:p.Ala4190=
XM_005262835.1:c.12570A>G XP_005262892.1:p.Ala4190=
XM_006714139.2:c.12570A>G XP_006714202.1:p.Ala4190=
XM_005262834.3:c.12570A>G XP_005262891.1:p.Ala4190=
XM_005262835.2:c.12570A>G XP_005262892.1:p.Ala4190=
XM_006714139.3:c.12570A>G XP_006714202.1:p.Ala4190=
NM_005245.4:c.12570A>G MANE Select NP_005236.2:p.Ala4190=