Canonical Allele Identifier: CA6227575

Gene: FAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92801167A>C , CM000673.2:g.92801167A>C	GRCh38
NC_000011.9:g.92534333A>C , CM000673.1:g.92534333A>C	GRCh37
NC_000011.8:g.92173981A>C	NCBI36
NG_052813.1:g.581532A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525166.6:c.8154A>C MANE Select	ENSP00000432586.2:p.Ala2718=
ENST00000409404.6:c.8154A>C	ENSP00000387040.2:p.Ala2718=
ENST00000525166.5:c.7704A>C	ENSP00000432586.1:p.Ala2568=
NM_001008781.2:c.8154A>C	NP_001008781.2:p.Ala2718=
XM_011542584.1:c.8268A>C	XP_011540886.1:p.Ala2756=
XM_017017178.2:c.8223A>C	XP_016872667.1:p.Ala2741=
XM_017017179.2:c.8223A>C	XP_016872668.1:p.Ala2741=
XM_017017180.1:c.8223A>C	XP_016872669.1:p.Ala2741=
XM_017017181.2:c.8154A>C	XP_016872670.1:p.Ala2718=
XM_017017182.2:c.8223A>C	XP_016872671.1:p.Ala2741=
XM_017017183.2:c.8154A>C	XP_016872672.1:p.Ala2718=
XM_017017184.2:c.8223A>C	XP_016872673.1:p.Ala2741=
XM_017017185.1:c.5007A>C	XP_016872674.1:p.Ala1669=
XM_017017186.1:c.4893A>C	XP_016872675.1:p.Ala1631=
XM_017017187.1:c.4893A>C	XP_016872676.1:p.Ala1631=
NM_001367949.1:c.8154A>C	NP_001354878.1:p.Ala2718=
NM_001367949.2:c.8154A>C MANE Select	NP_001354878.1:p.Ala2718=
NM_001008781.3:c.8154A>C	NP_001008781.2:p.Ala2718=