Canonical Allele Identifier: CA441374510

Gene: FAT4

Linked Data

• MyVariant Identifiers: chr4:g.126412707A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491552A>G , CM000666.2:g.125491552A>G	GRCh38
NC_000004.11:g.126412707A>G , CM000666.1:g.126412707A>G	GRCh37
NC_000004.10:g.126632157A>G	NCBI36
NG_033865.1:g.180141A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.14736A>G MANE Select	ENSP00000377862.4:p.Pro4912=
ENST00000674496.2:c.9507A>G	ENSP00000501473.2:p.Pro3169=
ENST00000335110.5:c.9453A>G	ENSP00000335169.5:p.Pro3151=
ENST00000394329.7:c.14730A>G	ENSP00000377862.3:p.Pro4910=
NM_001291285.1:c.14733A>G	NP_001278214.1:p.Pro4911=
NM_001291303.1:c.14736A>G	NP_001278232.1:p.Pro4912=
NM_024582.4:c.14730A>G	NP_078858.4:p.Pro4910=
XM_011532236.1:c.14736A>G	XP_011530538.1:p.Pro4912=
XM_011532237.1:c.9507A>G	XP_011530539.1:p.Pro3169=
XM_011532236.2:c.14736A>G	XP_011530538.1:p.Pro4912=
XM_011532237.2:c.9507A>G	XP_011530539.1:p.Pro3169=
NM_001291285.2:c.14733A>G	NP_001278214.1:p.Pro4911=
NM_001291303.3:c.14736A>G MANE Select	NP_001278232.1:p.Pro4912=
NM_024582.5:c.14730A>G	NP_078858.4:p.Pro4910=
NM_001291285.3:c.14733A>G	NP_001278214.1:p.Pro4911=
NM_024582.6:c.14730A>G	NP_078858.4:p.Pro4910=