Canonical Allele Identifier: CA358143774

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412802A>C (hg19) ; chr4:g.125491647A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491647A>C , CM000666.2:g.125491647A>C	GRCh38
NC_000004.11:g.126412802A>C , CM000666.1:g.126412802A>C	GRCh37
NC_000004.10:g.126632252A>C	NCBI36
NG_033865.1:g.180236A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14831A>C MANE Select	ENSP00000377862.4:p.His4944Pro
ENST00000674496.2:c.9602A>C	ENSP00000501473.2:p.His3201Pro
ENST00000335110.5:c.9548A>C	ENSP00000335169.5:p.His3183Pro
ENST00000394329.7:c.14825A>C	ENSP00000377862.3:p.His4942Pro
NM_001291285.1:c.14828A>C	NP_001278214.1:p.His4943Pro
NM_001291303.1:c.14831A>C	NP_001278232.1:p.His4944Pro
NM_024582.4:c.14825A>C	NP_078858.4:p.His4942Pro
XM_011532236.1:c.14831A>C	XP_011530538.1:p.His4944Pro
XM_011532237.1:c.9602A>C	XP_011530539.1:p.His3201Pro
XM_011532236.2:c.14831A>C	XP_011530538.1:p.His4944Pro
XM_011532237.2:c.9602A>C	XP_011530539.1:p.His3201Pro
NM_001291285.2:c.14828A>C	NP_001278214.1:p.His4943Pro
NM_001291303.3:c.14831A>C MANE Select	NP_001278232.1:p.His4944Pro
NM_024582.5:c.14825A>C	NP_078858.4:p.His4942Pro
NM_001291285.3:c.14828A>C	NP_001278214.1:p.His4943Pro
NM_024582.6:c.14825A>C	NP_078858.4:p.His4942Pro