Canonical Allele Identifier: CA358143770

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412801C>T (hg19) ; chr4:g.125491646C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491646C>T , CM000666.2:g.125491646C>T	GRCh38
NC_000004.11:g.126412801C>T , CM000666.1:g.126412801C>T	GRCh37
NC_000004.10:g.126632251C>T	NCBI36
NG_033865.1:g.180235C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14830C>T MANE Select	ENSP00000377862.4:p.His4944Tyr
ENST00000674496.2:c.9601C>T	ENSP00000501473.2:p.His3201Tyr
ENST00000335110.5:c.9547C>T	ENSP00000335169.5:p.His3183Tyr
ENST00000394329.7:c.14824C>T	ENSP00000377862.3:p.His4942Tyr
NM_001291285.1:c.14827C>T	NP_001278214.1:p.His4943Tyr
NM_001291303.1:c.14830C>T	NP_001278232.1:p.His4944Tyr
NM_024582.4:c.14824C>T	NP_078858.4:p.His4942Tyr
XM_011532236.1:c.14830C>T	XP_011530538.1:p.His4944Tyr
XM_011532237.1:c.9601C>T	XP_011530539.1:p.His3201Tyr
XM_011532236.2:c.14830C>T	XP_011530538.1:p.His4944Tyr
XM_011532237.2:c.9601C>T	XP_011530539.1:p.His3201Tyr
NM_001291285.2:c.14827C>T	NP_001278214.1:p.His4943Tyr
NM_001291303.3:c.14830C>T MANE Select	NP_001278232.1:p.His4944Tyr
NM_024582.5:c.14824C>T	NP_078858.4:p.His4942Tyr
NM_001291285.3:c.14827C>T	NP_001278214.1:p.His4943Tyr
NM_024582.6:c.14824C>T	NP_078858.4:p.His4942Tyr