Canonical Allele Identifier: CA358117505
Gene: FAT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317657A>T , CM000666.2:g.125317657A>T GRCh38
NC_000004.11:g.126238812A>T , CM000666.1:g.126238812A>T GRCh37
NC_000004.10:g.126458262A>T NCBI36
NG_033865.1:g.6246A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1246A>T MANE Select ENSP00000377862.4:p.Asn416Tyr
ENST00000674496.2:c.-55+1680A>T ENSP00000501473.2:p.=
ENST00000394329.7:c.1246A>T ENSP00000377862.3:p.Asn416Tyr
NM_001291285.1:n.1246A>T NP_001278214.1:p.Asn416Tyr
NM_001291303.1:n.1246A>T NP_001278232.1:p.Asn416Tyr
NM_024582.4:n.1246A>T NP_078858.4:p.Asn416Tyr
XM_011532236.1:c.1246A>T XP_011530538.1:p.Asn416Tyr
XM_011532237.1:c.-55+1680A>T XP_011530539.1:p.=
XM_011532236.2:c.1246A>T XP_011530538.1:p.Asn416Tyr
XM_011532237.2:c.-55+1680A>T XP_011530539.1:p.=
NM_001291285.2:c.1246A>T NP_001278214.1:p.Asn416Tyr
NM_001291303.3:c.1246A>T MANE Select NP_001278232.1:p.Asn416Tyr
NM_024582.5:c.1246A>T NP_078858.4:p.Asn416Tyr
NM_001291285.3:c.1246A>T NP_001278214.1:p.Asn416Tyr
NM_024582.6:c.1246A>T NP_078858.4:p.Asn416Tyr