Canonical Allele Identifier: CA6226344

Gene: FAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92353828C>T , CM000673.2:g.92353828C>T	GRCh38
NC_000011.9:g.92086994C>T , CM000673.1:g.92086994C>T	GRCh37
NC_000011.8:g.91726642C>T	NCBI36
NG_052813.1:g.134193C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001367949.2:c.1716C>T MANE Select	NP_001354878.1:p.Asn572=
ENST00000525166.6:c.1716C>T MANE Select	ENSP00000432586.2:p.Asn572=
NM_001008781.2:c.1716C>T	NP_001008781.2:p.Asn572=
NM_001008781.3:c.1716C>T	NP_001008781.2:p.Asn572=
NM_001367949.1:c.1716C>T	NP_001354878.1:p.Asn572=
NM_001378141.1:c.1716C>T	NP_001365070.1:p.Asn572=
ENST00000409404.6:c.1716C>T	ENSP00000387040.2:p.Asn572=
ENST00000525166.5:c.1266C>T	ENSP00000432586.1:p.Asn422=
XM_011542584.1:c.1761C>T	XP_011540886.1:p.Asn587=
XM_017017178.2:c.1716C>T	XP_016872667.1:p.Asn572=
XM_017017179.2:c.1716C>T	XP_016872668.1:p.Asn572=
XM_017017180.1:c.1716C>T	XP_016872669.1:p.Asn572=
XM_017017181.2:c.1716C>T	XP_016872670.1:p.Asn572=
XM_017017182.2:c.1716C>T	XP_016872671.1:p.Asn572=
XM_017017183.2:c.1716C>T	XP_016872672.1:p.Asn572=
XM_017017184.2:c.1716C>T	XP_016872673.1:p.Asn572=
XM_017017186.1:c.-39+128654C>T	XP_016872675.1:n.-39+128654C>T