Canonical Allele Identifier: CA1520091572

Gene: FAT1

Linked Data

• dbSNP Id: rs1738605450

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186597829T>A , CM000666.2:g.186597829T>A	GRCh38
NC_000004.11:g.187518983T>A , CM000666.1:g.187518983T>A	GRCh37
NC_000004.10:g.187755977T>A	NCBI36
NG_046994.1:g.134087A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441802.7:c.12258-37A>T MANE Select	ENSP00000406229.2:n.12258-37A>T
ENST00000441802.6:c.12258-37A>T	ENSP00000406229.2:n.12258-37A>T
ENST00000507105.1:c.54-37A>T
ENST00000507662.1:n.157-37A>T
ENST00000512347.1:n.450-37A>T
ENST00000614102.4:c.12264-37A>T	ENSP00000479573.1:n.12264-37A>T
NM_005245.3:c.12258-37A>T	NP_005236.2:n.12258-37A>T
XM_005262834.2:c.12258-37A>T	XP_005262891.1:n.12258-37A>T
XM_005262835.1:c.12258-37A>T	XP_005262892.1:n.12258-37A>T
XM_006714139.2:c.12258-37A>T	XP_006714202.1:n.12258-37A>T
XM_005262834.3:c.12258-37A>T	XP_005262891.1:n.12258-37A>T
XM_005262835.2:c.12258-37A>T	XP_005262892.1:n.12258-37A>T
XM_006714139.3:c.12258-37A>T	XP_006714202.1:n.12258-37A>T
NM_005245.4:c.12258-37A>T MANE Select	NP_005236.2:n.12258-37A>T