Canonical Allele Identifier: CA2672009308

Gene: FAT4

Linked Data

• gnomAD v4: 4-125317508-C-CGGTAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125317509_125317514dup , CM000666.2:g.125317509_125317514dup	GRCh38
NC_000004.11:g.126238664_126238669dup , CM000666.1:g.126238664_126238669dup	GRCh37
NC_000004.10:g.126458114_126458119dup	NCBI36
NG_033865.1:g.6098_6103dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.1098_1103dup MANE Select	ENSP00000377862.4:p.Val367_Asp368insGluVal
ENST00000674496.2:c.-55+1532_-55+1537dup	ENSP00000501473.2:n.-55+1532_-55+1537dup
ENST00000394329.7:c.1098_1103dup	ENSP00000377862.3:p.Val367_Asp368insGluVal
NM_001291285.1:c.1098_1103dup	NP_001278214.1:p.Val367_Asp368insGluVal
NM_001291303.1:c.1098_1103dup	NP_001278232.1:p.Val367_Asp368insGluVal
NM_024582.4:c.1098_1103dup	NP_078858.4:p.Val367_Asp368insGluVal
XM_011532236.1:c.1098_1103dup	XP_011530538.1:p.Val367_Asp368insGluVal
XM_011532237.1:c.-55+1532_-55+1537dup	XP_011530539.1:n.-55+1532_-55+1537dup
XM_011532236.2:c.1098_1103dup	XP_011530538.1:p.Val367_Asp368insGluVal
XM_011532237.2:c.-55+1532_-55+1537dup	XP_011530539.1:n.-55+1532_-55+1537dup
NM_001291285.2:c.1098_1103dup	NP_001278214.1:p.Val367_Asp368insGluVal
NM_001291303.3:c.1098_1103dup MANE Select	NP_001278232.1:p.Val367_Asp368insGluVal
NM_024582.5:c.1098_1103dup	NP_078858.4:p.Val367_Asp368insGluVal
NM_001291285.3:c.1098_1103dup	NP_001278214.1:p.Val367_Asp368insGluVal
NM_024582.6:c.1098_1103dup	NP_078858.4:p.Val367_Asp368insGluVal