Canonical Allele Identifier: CA358143749

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412792G>C (hg19) ; chr4:g.125491637G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491637G>C , CM000666.2:g.125491637G>C	GRCh38
NC_000004.11:g.126412792G>C , CM000666.1:g.126412792G>C	GRCh37
NC_000004.10:g.126632242G>C	NCBI36
NG_033865.1:g.180226G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14821G>C MANE Select	ENSP00000377862.4:p.Gly4941Arg
ENST00000674496.2:c.9592G>C	ENSP00000501473.2:p.Gly3198Arg
ENST00000335110.5:c.9538G>C	ENSP00000335169.5:p.Gly3180Arg
ENST00000394329.7:c.14815G>C	ENSP00000377862.3:p.Gly4939Arg
NM_001291285.1:c.14818G>C	NP_001278214.1:p.Gly4940Arg
NM_001291303.1:c.14821G>C	NP_001278232.1:p.Gly4941Arg
NM_024582.4:c.14815G>C	NP_078858.4:p.Gly4939Arg
XM_011532236.1:c.14821G>C	XP_011530538.1:p.Gly4941Arg
XM_011532237.1:c.9592G>C	XP_011530539.1:p.Gly3198Arg
XM_011532236.2:c.14821G>C	XP_011530538.1:p.Gly4941Arg
XM_011532237.2:c.9592G>C	XP_011530539.1:p.Gly3198Arg
NM_001291285.2:c.14818G>C	NP_001278214.1:p.Gly4940Arg
NM_001291303.3:c.14821G>C MANE Select	NP_001278232.1:p.Gly4941Arg
NM_024582.5:c.14815G>C	NP_078858.4:p.Gly4939Arg
NM_001291285.3:c.14818G>C	NP_001278214.1:p.Gly4940Arg
NM_024582.6:c.14815G>C	NP_078858.4:p.Gly4939Arg