Canonical Allele Identifier: CA3074222
Community Standard Title: NM_001291303.3(FAT4):c.12910G>A (p.Gly4304Ser)
Gene: FAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125487432G>A , CM000666.2:g.125487432G>A GRCh38
NC_000004.11:g.126408587G>A , CM000666.1:g.126408587G>A GRCh37
NC_000004.10:g.126628037G>A NCBI36
NG_033865.1:g.176021G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001291303.3:c.12910G>A MANE Select NP_001278232.1:p.Gly4304Ser
ENST00000394329.9:c.12910G>A MANE Select ENSP00000377862.4:p.Gly4304Ser
NM_001291285.1:c.12910G>A NP_001278214.1:p.Gly4304Ser
NM_001291285.2:c.12910G>A NP_001278214.1:p.Gly4304Ser
NM_001291285.3:c.12910G>A NP_001278214.1:p.Gly4304Ser
NM_001291303.1:c.12910G>A NP_001278232.1:p.Gly4304Ser
NM_024582.4:c.12904G>A NP_078858.4:p.Gly4302Ser
NM_024582.5:c.12904G>A NP_078858.4:p.Gly4302Ser
NM_024582.6:c.12904G>A NP_078858.4:p.Gly4302Ser
ENST00000335110.5:c.7627G>A ENSP00000335169.5:p.Gly2543Ser
ENST00000394329.7:c.12904G>A ENSP00000377862.3:p.Gly4302Ser
ENST00000674496.2:c.7681G>A ENSP00000501473.2:p.Gly2561Ser
XM_011532236.1:c.12910G>A XP_011530538.1:p.Gly4304Ser
XM_011532236.2:c.12910G>A XP_011530538.1:p.Gly4304Ser
XM_011532237.1:c.7681G>A XP_011530539.1:p.Gly2561Ser
XM_011532237.2:c.7681G>A XP_011530539.1:p.Gly2561Ser