Canonical Allele Identifier: CA441374523

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412713T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491558T>G , CM000666.2:g.125491558T>G	GRCh38
NC_000004.11:g.126412713T>G , CM000666.1:g.126412713T>G	GRCh37
NC_000004.10:g.126632163T>G	NCBI36
NG_033865.1:g.180147T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14742T>G MANE Select	ENSP00000377862.4:p.Thr4914=
ENST00000674496.2:c.9513T>G	ENSP00000501473.2:p.Thr3171=
ENST00000335110.5:c.9459T>G	ENSP00000335169.5:p.Thr3153=
ENST00000394329.7:c.14736T>G	ENSP00000377862.3:p.Thr4912=
NM_001291285.1:c.14739T>G	NP_001278214.1:p.Thr4913=
NM_001291303.1:c.14742T>G	NP_001278232.1:p.Thr4914=
NM_024582.4:c.14736T>G	NP_078858.4:p.Thr4912=
XM_011532236.1:c.14742T>G	XP_011530538.1:p.Thr4914=
XM_011532237.1:c.9513T>G	XP_011530539.1:p.Thr3171=
XM_011532236.2:c.14742T>G	XP_011530538.1:p.Thr4914=
XM_011532237.2:c.9513T>G	XP_011530539.1:p.Thr3171=
NM_001291285.2:c.14739T>G	NP_001278214.1:p.Thr4913=
NM_001291303.3:c.14742T>G MANE Select	NP_001278232.1:p.Thr4914=
NM_024582.5:c.14736T>G	NP_078858.4:p.Thr4912=
NM_001291285.3:c.14739T>G	NP_001278214.1:p.Thr4913=
NM_024582.6:c.14736T>G	NP_078858.4:p.Thr4912=