Canonical Allele Identifier: CA3074439

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125490623A>G , CM000666.2:g.125490623A>G	GRCh38
NC_000004.11:g.126411778A>G , CM000666.1:g.126411778A>G	GRCh37
NC_000004.10:g.126631228A>G	NCBI36
NG_033865.1:g.179212A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.13807A>G MANE Select	NP_001278232.1:p.Asn4603Asp
ENST00000394329.9:c.13807A>G MANE Select	ENSP00000377862.4:p.Asn4603Asp
NM_001291285.1:c.13804A>G	NP_001278214.1:p.Asn4602Asp
NM_001291285.2:c.13804A>G	NP_001278214.1:p.Asn4602Asp
NM_001291285.3:c.13804A>G	NP_001278214.1:p.Asn4602Asp
NM_001291303.1:c.13807A>G	NP_001278232.1:p.Asn4603Asp
NM_024582.4:c.13801A>G	NP_078858.4:p.Asn4601Asp
NM_024582.5:c.13801A>G	NP_078858.4:p.Asn4601Asp
NM_024582.6:c.13801A>G	NP_078858.4:p.Asn4601Asp
ENST00000335110.5:c.8524A>G	ENSP00000335169.5:p.Asn2842Asp
ENST00000394329.7:c.13801A>G	ENSP00000377862.3:p.Asn4601Asp
ENST00000674496.2:c.8578A>G	ENSP00000501473.2:p.Asn2860Asp
XM_011532236.1:c.13807A>G	XP_011530538.1:p.Asn4603Asp
XM_011532236.2:c.13807A>G	XP_011530538.1:p.Asn4603Asp
XM_011532237.1:c.8578A>G	XP_011530539.1:p.Asn2860Asp
XM_011532237.2:c.8578A>G	XP_011530539.1:p.Asn2860Asp