Canonical Allele Identifier: CA441366875
Gene: FAT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.126238805A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317650A>G , CM000666.2:g.125317650A>G GRCh38
NC_000004.11:g.126238805A>G , CM000666.1:g.126238805A>G GRCh37
NC_000004.10:g.126458255A>G NCBI36
NG_033865.1:g.6239A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000394329.9:c.1239A>G MANE Select ENSP00000377862.4:p.Lys413=
ENST00000674496.2:c.-55+1673A>G ENSP00000501473.2:p.=
ENST00000394329.7:c.1239A>G ENSP00000377862.3:p.Lys413=
NM_001291285.1:n.1239A>G NP_001278214.1:p.Lys413=
NM_001291303.1:n.1239A>G NP_001278232.1:p.Lys413=
NM_024582.4:n.1239A>G NP_078858.4:p.Lys413=
XM_011532236.1:c.1239A>G XP_011530538.1:p.Lys413=
XM_011532237.1:c.-55+1673A>G XP_011530539.1:p.=
XM_011532236.2:c.1239A>G XP_011530538.1:p.Lys413=
XM_011532237.2:c.-55+1673A>G XP_011530539.1:p.=
NM_001291285.2:c.1239A>G NP_001278214.1:p.Lys413=
NM_001291303.3:c.1239A>G MANE Select NP_001278232.1:p.Lys413=
NM_024582.5:c.1239A>G NP_078858.4:p.Lys413=
NM_001291285.3:c.1239A>G NP_001278214.1:p.Lys413=
NM_024582.6:c.1239A>G NP_078858.4:p.Lys413=