Canonical Allele Identifier: CA358128444
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs1085307886
MyVariant Identifiers: chr4:g.126389852G>A (hg19) chr4:g.125468697G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125468697G>A , CM000666.2:g.125468697G>A GRCh38
NC_000004.11:g.126389852G>A , CM000666.1:g.126389852G>A GRCh37
NC_000004.10:g.126609302G>A NCBI36
NG_033865.1:g.157286G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.12091G>A MANE Select ENSP00000377862.4:p.Glu4031Lys
ENST00000674496.2:c.6862G>A ENSP00000501473.2:p.Glu2288Lys
ENST00000335110.5:c.6874G>A ENSP00000335169.5:p.Glu2292Lys
ENST00000394329.7:c.12085G>A ENSP00000377862.3:p.Glu4029Lys
NM_001291285.1:c.12091G>A NP_001278214.1:p.Glu4031Lys
NM_001291303.1:c.12091G>A NP_001278232.1:p.Glu4031Lys
NM_024582.4:c.12085G>A NP_078858.4:p.Glu4029Lys
XM_011532236.1:c.12091G>A XP_011530538.1:p.Glu4031Lys
XM_011532237.1:c.6862G>A XP_011530539.1:p.Glu2288Lys
XM_011532236.2:c.12091G>A XP_011530538.1:p.Glu4031Lys
XM_011532237.2:c.6862G>A XP_011530539.1:p.Glu2288Lys
NM_001291285.2:c.12091G>A NP_001278214.1:p.Glu4031Lys
NM_001291303.3:c.12091G>A MANE Select NP_001278232.1:p.Glu4031Lys
NM_024582.5:c.12085G>A NP_078858.4:p.Glu4029Lys
NM_001291285.3:c.12091G>A NP_001278214.1:p.Glu4031Lys
NM_024582.6:c.12085G>A NP_078858.4:p.Glu4029Lys
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