Canonical Allele Identifier: CA358117414
Gene: FAT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.125317617T>A , CM000666.2:g.125317617T>A GRCh38
NC_000004.11:g.126238772T>A , CM000666.1:g.126238772T>A GRCh37
NC_000004.10:g.126458222T>A NCBI36
NG_033865.1:g.6206T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394329.9:c.1206T>A MANE Select ENSP00000377862.4:p.Asn402Lys
ENST00000674496.2:c.-55+1640T>A ENSP00000501473.2:n.-55+1640T>A
ENST00000394329.7:c.1206T>A ENSP00000377862.3:p.Asn402Lys
NM_001291285.1:c.1206T>A NP_001278214.1:p.Asn402Lys
NM_001291303.1:c.1206T>A NP_001278232.1:p.Asn402Lys
NM_024582.4:c.1206T>A NP_078858.4:p.Asn402Lys
XM_011532236.1:c.1206T>A XP_011530538.1:p.Asn402Lys
XM_011532237.1:c.-55+1640T>A XP_011530539.1:n.-55+1640T>A
XM_011532236.2:c.1206T>A XP_011530538.1:p.Asn402Lys
XM_011532237.2:c.-55+1640T>A XP_011530539.1:n.-55+1640T>A
NM_001291285.2:c.1206T>A NP_001278214.1:p.Asn402Lys
NM_001291303.3:c.1206T>A MANE Select NP_001278232.1:p.Asn402Lys
NM_024582.5:c.1206T>A NP_078858.4:p.Asn402Lys
NM_001291285.3:c.1206T>A NP_001278214.1:p.Asn402Lys
NM_024582.6:c.1206T>A NP_078858.4:p.Asn402Lys