Canonical Allele Identifier: CA441373853

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412809A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491654A>C , CM000666.2:g.125491654A>C	GRCh38
NC_000004.11:g.126412809A>C , CM000666.1:g.126412809A>C	GRCh37
NC_000004.10:g.126632259A>C	NCBI36
NG_033865.1:g.180243A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14838A>C MANE Select	ENSP00000377862.4:p.Val4946=
ENST00000674496.2:c.9609A>C	ENSP00000501473.2:p.Val3203=
ENST00000335110.5:c.9555A>C	ENSP00000335169.5:p.Val3185=
ENST00000394329.7:c.14832A>C	ENSP00000377862.3:p.Val4944=
NM_001291285.1:c.14835A>C	NP_001278214.1:p.Val4945=
NM_001291303.1:c.14838A>C	NP_001278232.1:p.Val4946=
NM_024582.4:c.14832A>C	NP_078858.4:p.Val4944=
XM_011532236.1:c.14838A>C	XP_011530538.1:p.Val4946=
XM_011532237.1:c.9609A>C	XP_011530539.1:p.Val3203=
XM_011532236.2:c.14838A>C	XP_011530538.1:p.Val4946=
XM_011532237.2:c.9609A>C	XP_011530539.1:p.Val3203=
NM_001291285.2:c.14835A>C	NP_001278214.1:p.Val4945=
NM_001291303.3:c.14838A>C MANE Select	NP_001278232.1:p.Val4946=
NM_024582.5:c.14832A>C	NP_078858.4:p.Val4944=
NM_001291285.3:c.14835A>C	NP_001278214.1:p.Val4945=
NM_024582.6:c.14832A>C	NP_078858.4:p.Val4944=