Canonical Allele Identifier: CA3165478
Community Standard Title: NM_005245.4(FAT1):c.10079A>G (p.Asp3360Gly)
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186609310T>C , CM000666.2:g.186609310T>C GRCh38
NC_000004.11:g.187530464T>C , CM000666.1:g.187530464T>C GRCh37
NC_000004.10:g.187767458T>C NCBI36
NG_046994.1:g.122606A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005245.4:c.10079A>G MANE Select NP_005236.2:p.Asp3360Gly
ENST00000441802.7:c.10079A>G MANE Select ENSP00000406229.2:p.Asp3360Gly
NM_005245.3:c.10079A>G NP_005236.2:p.Asp3360Gly
ENST00000441802.6:c.10079A>G ENSP00000406229.2:p.Asp3360Gly
ENST00000508035.1:n.281A>G
ENST00000614102.4:c.10085A>G ENSP00000479573.1:p.Asp3362Gly
XM_005262834.2:c.10079A>G XP_005262891.1:p.Asp3360Gly
XM_005262834.3:c.10079A>G XP_005262891.1:p.Asp3360Gly
XM_005262835.1:c.10079A>G XP_005262892.1:p.Asp3360Gly
XM_005262835.2:c.10079A>G XP_005262892.1:p.Asp3360Gly
XM_006714139.2:c.10079A>G XP_006714202.1:p.Asp3360Gly
XM_006714139.3:c.10079A>G XP_006714202.1:p.Asp3360Gly