Canonical Allele Identifier: CA6227349

Gene: FAT3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.92799799C>T , CM000673.2:g.92799799C>T	GRCh38
NC_000011.9:g.92532965C>T , CM000673.1:g.92532965C>T	GRCh37
NC_000011.8:g.92172613C>T	NCBI36
NG_052813.1:g.580164C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525166.6:c.6786C>T MANE Select	ENSP00000432586.2:p.Asp2262=
ENST00000409404.6:c.6786C>T	ENSP00000387040.2:p.Asp2262=
ENST00000525166.5:c.6336C>T	ENSP00000432586.1:p.Asp2112=
NM_001008781.2:c.6786C>T	NP_001008781.2:p.Asp2262=
XM_011542584.1:c.6900C>T	XP_011540886.1:p.Asp2300=
XM_017017178.2:c.6855C>T	XP_016872667.1:p.Asp2285=
XM_017017179.2:c.6855C>T	XP_016872668.1:p.Asp2285=
XM_017017180.1:c.6855C>T	XP_016872669.1:p.Asp2285=
XM_017017181.2:c.6786C>T	XP_016872670.1:p.Asp2262=
XM_017017182.2:c.6855C>T	XP_016872671.1:p.Asp2285=
XM_017017183.2:c.6786C>T	XP_016872672.1:p.Asp2262=
XM_017017184.2:c.6855C>T	XP_016872673.1:p.Asp2285=
XM_017017185.1:c.3639C>T	XP_016872674.1:p.Asp1213=
XM_017017186.1:c.3525C>T	XP_016872675.1:p.Asp1175=
XM_017017187.1:c.3525C>T	XP_016872676.1:p.Asp1175=
NM_001367949.1:c.6786C>T	NP_001354878.1:p.Asp2262=
NM_001367949.2:c.6786C>T MANE Select	NP_001354878.1:p.Asp2262=
NM_001008781.3:c.6786C>T	NP_001008781.2:p.Asp2262=