Canonical Allele Identifier: CA3167630
Community Standard Title: NM_005245.4(FAT1):c.635A>T (p.Tyr212Phe)
Gene: FAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186709193T>A , CM000666.2:g.186709193T>A GRCh38
NC_000004.11:g.187630347T>A , CM000666.1:g.187630347T>A GRCh37
NC_000004.10:g.187867341T>A NCBI36
NG_046994.1:g.22723A>T

Transcript Alleles

HGVS Amino-acid Change
NM_005245.4:c.635A>T MANE Select NP_005236.2:p.Tyr212Phe
ENST00000441802.7:c.635A>T MANE Select ENSP00000406229.2:p.Tyr212Phe
NM_005245.3:c.635A>T NP_005236.2:p.Tyr212Phe
ENST00000441802.6:c.635A>T ENSP00000406229.2:p.Tyr212Phe
ENST00000509647.1:c.635A>T ENSP00000423736.1:p.Tyr212Phe
ENST00000614102.4:c.635A>T ENSP00000479573.1:p.Tyr212Phe
XM_005262834.2:c.635A>T XP_005262891.1:p.Tyr212Phe
XM_005262834.3:c.635A>T XP_005262891.1:p.Tyr212Phe
XM_005262835.1:c.635A>T XP_005262892.1:p.Tyr212Phe
XM_005262835.2:c.635A>T XP_005262892.1:p.Tyr212Phe
XM_006714139.2:c.635A>T XP_006714202.1:p.Tyr212Phe
XM_006714139.3:c.635A>T XP_006714202.1:p.Tyr212Phe