Canonical Allele Identifier: CA441205038

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126355515A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434360A>T , CM000666.2:g.125434360A>T	GRCh38
NC_000004.11:g.126355515A>T , CM000666.1:g.126355515A>T	GRCh37
NC_000004.10:g.126574965A>T	NCBI36
NG_033865.1:g.122949A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7134A>T MANE Select	ENSP00000377862.4:p.Pro2378=
ENST00000674496.2:c.1905A>T	ENSP00000501473.2:p.Pro635=
ENST00000335110.5:c.2028A>T	ENSP00000335169.5:p.Pro676=
ENST00000394329.7:c.7134A>T	ENSP00000377862.3:p.Pro2378=
NM_001291285.1:c.7134A>T	NP_001278214.1:p.Pro2378=
NM_001291303.1:c.7134A>T	NP_001278232.1:p.Pro2378=
NM_024582.4:c.7134A>T	NP_078858.4:p.Pro2378=
XM_011532236.1:c.7134A>T	XP_011530538.1:p.Pro2378=
XM_011532237.1:c.1905A>T	XP_011530539.1:p.Pro635=
XM_011532236.2:c.7134A>T	XP_011530538.1:p.Pro2378=
XM_011532237.2:c.1905A>T	XP_011530539.1:p.Pro635=
NM_001291285.2:c.7134A>T	NP_001278214.1:p.Pro2378=
NM_001291303.3:c.7134A>T MANE Select	NP_001278232.1:p.Pro2378=
NM_024582.5:c.7134A>T	NP_078858.4:p.Pro2378=
NM_001291285.3:c.7134A>T	NP_001278214.1:p.Pro2378=
NM_024582.6:c.7134A>T	NP_078858.4:p.Pro2378=