Canonical Allele Identifier: CA2708139691

Gene: FAT1

Linked Data

• dbSNP Id: rs2126400397

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186597822_186597823insACGATCCTA , CM000666.2:g.186597822_186597823insACGATCCTA	GRCh38
NC_000004.11:g.187518976_187518977insACGATCCTA , CM000666.1:g.187518976_187518977insACGATCCTA	GRCh37
NC_000004.10:g.187755970_187755971insACGATCCTA	NCBI36
NG_046994.1:g.134093_134094insTAGGATCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441802.7:c.12258-31_12258-30insTAGGATCGT MANE Select	ENSP00000406229.2:n.12258-31_12258-30insTAGGATCGT
ENST00000441802.6:c.12258-31_12258-30insTAGGATCGT	ENSP00000406229.2:n.12258-31_12258-30insTAGGATCGT
ENST00000507105.1:c.54-31_54-30insTAGGATCGT
ENST00000507662.1:n.157-31_157-30insTAGGATCGT
ENST00000512347.1:n.450-31_450-30insTAGGATCGT
ENST00000614102.4:c.12264-31_12264-30insTAGGATCGT	ENSP00000479573.1:n.12264-31_12264-30insTAGGATCGT
NM_005245.3:c.12258-31_12258-30insTAGGATCGT	NP_005236.2:n.12258-31_12258-30insTAGGATCGT
XM_005262834.2:c.12258-31_12258-30insTAGGATCGT	XP_005262891.1:n.12258-31_12258-30insTAGGATCGT
XM_005262835.1:c.12258-31_12258-30insTAGGATCGT	XP_005262892.1:n.12258-31_12258-30insTAGGATCGT
XM_006714139.2:c.12258-31_12258-30insTAGGATCGT	XP_006714202.1:n.12258-31_12258-30insTAGGATCGT
XM_005262834.3:c.12258-31_12258-30insTAGGATCGT	XP_005262891.1:n.12258-31_12258-30insTAGGATCGT
XM_005262835.2:c.12258-31_12258-30insTAGGATCGT	XP_005262892.1:n.12258-31_12258-30insTAGGATCGT
XM_006714139.3:c.12258-31_12258-30insTAGGATCGT	XP_006714202.1:n.12258-31_12258-30insTAGGATCGT
NM_005245.4:c.12258-31_12258-30insTAGGATCGT MANE Select	NP_005236.2:n.12258-31_12258-30insTAGGATCGT