Canonical Allele Identifier: CA1491680519
Gene: FAT4 HGNC NCBI

Linked Data

dbSNP Id: rs1727652563

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125491663dup , CM000666.2:g.125491663dup GRCh38
NC_000004.11:g.126412818dup , CM000666.1:g.126412818dup GRCh37
NC_000004.10:g.126632268dup NCBI36
NG_033865.1:g.180252dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.14847dup MANE Select ENSP00000377862.4:p.Lys4950Ter
ENST00000674496.2:c.9618dup ENSP00000501473.2:p.Lys3207Ter
ENST00000335110.5:c.9564dup ENSP00000335169.5:p.Lys3189Ter
ENST00000394329.7:c.14841dup ENSP00000377862.3:p.Lys4948Ter
NM_001291285.1:c.14844dup NP_001278214.1:p.Lys4949Ter
NM_001291303.1:c.14847dup NP_001278232.1:p.Lys4950Ter
NM_024582.4:c.14841dup NP_078858.4:p.Lys4948Ter
XM_011532236.1:c.14847dup XP_011530538.1:p.Lys4950Ter
XM_011532237.1:c.9618dup XP_011530539.1:p.Lys3207Ter
XM_011532236.2:c.14847dup XP_011530538.1:p.Lys4950Ter
XM_011532237.2:c.9618dup XP_011530539.1:p.Lys3207Ter
NM_001291285.2:c.14844dup NP_001278214.1:p.Lys4949Ter
NM_001291303.3:c.14847dup MANE Select NP_001278232.1:p.Lys4950Ter
NM_024582.5:c.14841dup NP_078858.4:p.Lys4948Ter
NM_001291285.3:c.14844dup NP_001278214.1:p.Lys4949Ter
NM_024582.6:c.14841dup NP_078858.4:p.Lys4948Ter