Canonical Allele Identifier: CA441205049

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355530T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434375T>C , CM000666.2:g.125434375T>C	GRCh38
NC_000004.11:g.126355530T>C , CM000666.1:g.126355530T>C	GRCh37
NC_000004.10:g.126574980T>C	NCBI36
NG_033865.1:g.122964T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7149T>C MANE Select	ENSP00000377862.4:p.Val2383=
ENST00000674496.2:c.1920T>C	ENSP00000501473.2:p.Val640=
ENST00000335110.5:c.2043T>C	ENSP00000335169.5:p.Val681=
ENST00000394329.7:c.7149T>C	ENSP00000377862.3:p.Val2383=
NM_001291285.1:c.7149T>C	NP_001278214.1:p.Val2383=
NM_001291303.1:c.7149T>C	NP_001278232.1:p.Val2383=
NM_024582.4:c.7149T>C	NP_078858.4:p.Val2383=
XM_011532236.1:c.7149T>C	XP_011530538.1:p.Val2383=
XM_011532237.1:c.1920T>C	XP_011530539.1:p.Val640=
XM_011532236.2:c.7149T>C	XP_011530538.1:p.Val2383=
XM_011532237.2:c.1920T>C	XP_011530539.1:p.Val640=
NM_001291285.2:c.7149T>C	NP_001278214.1:p.Val2383=
NM_001291303.3:c.7149T>C MANE Select	NP_001278232.1:p.Val2383=
NM_024582.5:c.7149T>C	NP_078858.4:p.Val2383=
NM_001291285.3:c.7149T>C	NP_001278214.1:p.Val2383=
NM_024582.6:c.7149T>C	NP_078858.4:p.Val2383=