Canonical Allele Identifier: CA786679093

Gene: FAT4

Linked Data

• dbSNP Id: rs1213572045
• MyVariant Identifiers: chr4:g.126412812_126412814del (hg19) ; chr4:g.125491657_125491659del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491658_125491660del , CM000666.2:g.125491658_125491660del	GRCh38
NC_000004.11:g.126412813_126412815del , CM000666.1:g.126412813_126412815del	GRCh37
NC_000004.10:g.126632263_126632265del	NCBI36
NG_033865.1:g.180247_180249del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14842_14844del MANE Select	ENSP00000377862.4:p.Val4948del
ENST00000674496.2:c.9613_9615del	ENSP00000501473.2:p.Val3205del
ENST00000335110.5:c.9559_9561del	ENSP00000335169.5:p.Val3187del
ENST00000394329.7:c.14836_14838del	ENSP00000377862.3:p.Val4946del
NM_001291285.1:c.14839_14841del	NP_001278214.1:p.Val4947del
NM_001291303.1:c.14842_14844del	NP_001278232.1:p.Val4948del
NM_024582.4:c.14836_14838del	NP_078858.4:p.Val4946del
XM_011532236.1:c.14842_14844del	XP_011530538.1:p.Val4948del
XM_011532237.1:c.9613_9615del	XP_011530539.1:p.Val3205del
XM_011532236.2:c.14842_14844del	XP_011530538.1:p.Val4948del
XM_011532237.2:c.9613_9615del	XP_011530539.1:p.Val3205del
NM_001291285.2:c.14839_14841del	NP_001278214.1:p.Val4947del
NM_001291303.3:c.14842_14844del MANE Select	NP_001278232.1:p.Val4948del
NM_024582.5:c.14836_14838del	NP_078858.4:p.Val4946del
NM_001291285.3:c.14839_14841del	NP_001278214.1:p.Val4947del
NM_024582.6:c.14836_14838del	NP_078858.4:p.Val4946del