Canonical Allele Identifier: CA3167447
Community Standard Title: NM_005245.4(FAT1):c.1532C>T (p.Ala511Val)
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186708296G>A , CM000666.2:g.186708296G>A GRCh38
NC_000004.11:g.187629450G>A , CM000666.1:g.187629450G>A GRCh37
NC_000004.10:g.187866444G>A NCBI36
NG_046994.1:g.23620C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005245.4:c.1532C>T MANE Select NP_005236.2:p.Ala511Val
ENST00000441802.7:c.1532C>T MANE Select ENSP00000406229.2:p.Ala511Val
NM_005245.3:c.1532C>T NP_005236.2:p.Ala511Val
ENST00000441802.6:c.1532C>T ENSP00000406229.2:p.Ala511Val
ENST00000614102.4:c.1532C>T ENSP00000479573.1:p.Ala511Val
XM_005262834.2:c.1532C>T XP_005262891.1:p.Ala511Val
XM_005262834.3:c.1532C>T XP_005262891.1:p.Ala511Val
XM_005262835.1:c.1532C>T XP_005262892.1:p.Ala511Val
XM_005262835.2:c.1532C>T XP_005262892.1:p.Ala511Val
XM_006714139.2:c.1532C>T XP_006714202.1:p.Ala511Val
XM_006714139.3:c.1532C>T XP_006714202.1:p.Ala511Val