Canonical Allele Identifier: CA3164918
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186598064C>G , CM000666.2:g.186598064C>G GRCh38
NC_000004.11:g.187519218C>G , CM000666.1:g.187519218C>G GRCh37
NC_000004.10:g.187756212C>G NCBI36
NG_046994.1:g.133852G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441802.7:c.12165G>C MANE Select ENSP00000406229.2:p.Pro4055=
ENST00000441802.6:c.12165G>C ENSP00000406229.2:p.Pro4055=
ENST00000507662.1:n.64G>C
ENST00000512347.1:n.357G>C
ENST00000614102.4:c.12171G>C ENSP00000479573.1:p.Pro4057=
NM_005245.3:c.12165G>C NP_005236.2:p.Pro4055=
XM_005262834.2:c.12165G>C XP_005262891.1:p.Pro4055=
XM_005262835.1:c.12165G>C XP_005262892.1:p.Pro4055=
XM_006714139.2:c.12165G>C XP_006714202.1:p.Pro4055=
XM_005262834.3:c.12165G>C XP_005262891.1:p.Pro4055=
XM_005262835.2:c.12165G>C XP_005262892.1:p.Pro4055=
XM_006714139.3:c.12165G>C XP_006714202.1:p.Pro4055=
NM_005245.4:c.12165G>C MANE Select NP_005236.2:p.Pro4055=