Canonical Allele Identifier: CA1520091575

Gene: FAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186597831C= , CM000666.2:g.186597831C=	GRCh38
NC_000004.11:g.187518985C= , CM000666.1:g.187518985C=	GRCh37
NC_000004.10:g.187755979C=	NCBI36
NG_046994.1:g.134085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441802.7:c.12258-39G= MANE Select	ENSP00000406229.2:n.12258-39G=
ENST00000441802.6:c.12258-39G=	ENSP00000406229.2:n.12258-39G=
ENST00000507105.1:c.54-39G=
ENST00000507662.1:n.157-39G=
ENST00000512347.1:n.450-39G=
ENST00000614102.4:c.12264-39G=	ENSP00000479573.1:n.12264-39G=
NM_005245.3:c.12258-39G=	NP_005236.2:n.12258-39G=
XM_005262834.2:c.12258-39G=	XP_005262891.1:n.12258-39G=
XM_005262835.1:c.12258-39G=	XP_005262892.1:n.12258-39G=
XM_006714139.2:c.12258-39G=	XP_006714202.1:n.12258-39G=
XM_005262834.3:c.12258-39G=	XP_005262891.1:n.12258-39G=
XM_005262835.2:c.12258-39G=	XP_005262892.1:n.12258-39G=
XM_006714139.3:c.12258-39G=	XP_006714202.1:n.12258-39G=
NM_005245.4:c.12258-39G= MANE Select	NP_005236.2:n.12258-39G=