Canonical Allele Identifier: CA358135441

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355550A>C (hg19) ; chr4:g.125434395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434395A>C , CM000666.2:g.125434395A>C	GRCh38
NC_000004.11:g.126355550A>C , CM000666.1:g.126355550A>C	GRCh37
NC_000004.10:g.126575000A>C	NCBI36
NG_033865.1:g.122984A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7169A>C MANE Select	ENSP00000377862.4:p.Asp2390Ala
ENST00000674496.2:c.1940A>C	ENSP00000501473.2:p.Asp647Ala
ENST00000335110.5:c.2063A>C	ENSP00000335169.5:p.Asp688Ala
ENST00000394329.7:c.7169A>C	ENSP00000377862.3:p.Asp2390Ala
NM_001291285.1:c.7169A>C	NP_001278214.1:p.Asp2390Ala
NM_001291303.1:c.7169A>C	NP_001278232.1:p.Asp2390Ala
NM_024582.4:c.7169A>C	NP_078858.4:p.Asp2390Ala
XM_011532236.1:c.7169A>C	XP_011530538.1:p.Asp2390Ala
XM_011532237.1:c.1940A>C	XP_011530539.1:p.Asp647Ala
XM_011532236.2:c.7169A>C	XP_011530538.1:p.Asp2390Ala
XM_011532237.2:c.1940A>C	XP_011530539.1:p.Asp647Ala
NM_001291285.2:c.7169A>C	NP_001278214.1:p.Asp2390Ala
NM_001291303.3:c.7169A>C MANE Select	NP_001278232.1:p.Asp2390Ala
NM_024582.5:c.7169A>C	NP_078858.4:p.Asp2390Ala
NM_001291285.3:c.7169A>C	NP_001278214.1:p.Asp2390Ala
NM_024582.6:c.7169A>C	NP_078858.4:p.Asp2390Ala