Canonical Allele Identifier: CA358143759

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412796T>C (hg19) ; chr4:g.125491641T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491641T>C , CM000666.2:g.125491641T>C	GRCh38
NC_000004.11:g.126412796T>C , CM000666.1:g.126412796T>C	GRCh37
NC_000004.10:g.126632246T>C	NCBI36
NG_033865.1:g.180230T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14825T>C MANE Select	ENSP00000377862.4:p.Phe4942Ser
ENST00000674496.2:c.9596T>C	ENSP00000501473.2:p.Phe3199Ser
ENST00000335110.5:c.9542T>C	ENSP00000335169.5:p.Phe3181Ser
ENST00000394329.7:c.14819T>C	ENSP00000377862.3:p.Phe4940Ser
NM_001291285.1:c.14822T>C	NP_001278214.1:p.Phe4941Ser
NM_001291303.1:c.14825T>C	NP_001278232.1:p.Phe4942Ser
NM_024582.4:c.14819T>C	NP_078858.4:p.Phe4940Ser
XM_011532236.1:c.14825T>C	XP_011530538.1:p.Phe4942Ser
XM_011532237.1:c.9596T>C	XP_011530539.1:p.Phe3199Ser
XM_011532236.2:c.14825T>C	XP_011530538.1:p.Phe4942Ser
XM_011532237.2:c.9596T>C	XP_011530539.1:p.Phe3199Ser
NM_001291285.2:c.14822T>C	NP_001278214.1:p.Phe4941Ser
NM_001291303.3:c.14825T>C MANE Select	NP_001278232.1:p.Phe4942Ser
NM_024582.5:c.14819T>C	NP_078858.4:p.Phe4940Ser
NM_001291285.3:c.14822T>C	NP_001278214.1:p.Phe4941Ser
NM_024582.6:c.14819T>C	NP_078858.4:p.Phe4940Ser