Canonical Allele Identifier: CA1520091580

Gene: FAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186597841_186597842delinsTA , CM000666.2:g.186597841_186597842delinsTA	GRCh38
NC_000004.11:g.187518995_187518996delinsTA , CM000666.1:g.187518995_187518996delinsTA	GRCh37
NC_000004.10:g.187755989_187755990delinsTA	NCBI36
NG_046994.1:g.134074_134075delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000441802.7:c.12258-50_12258-49delinsTA MANE Select	ENSP00000406229.2:n.12258-50_12258-49delinsTA
ENST00000441802.6:c.12258-50_12258-49delinsTA	ENSP00000406229.2:n.12258-50_12258-49delinsTA
ENST00000507105.1:c.54-50_54-49delinsTA
ENST00000507662.1:n.157-50_157-49delinsTA
ENST00000512347.1:n.450-50_450-49delinsTA
ENST00000614102.4:c.12264-50_12264-49delinsTA	ENSP00000479573.1:n.12264-50_12264-49delinsTA
NM_005245.3:c.12258-50_12258-49delinsTA	NP_005236.2:n.12258-50_12258-49delinsTA
XM_005262834.2:c.12258-50_12258-49delinsTA	XP_005262891.1:n.12258-50_12258-49delinsTA
XM_005262835.1:c.12258-50_12258-49delinsTA	XP_005262892.1:n.12258-50_12258-49delinsTA
XM_006714139.2:c.12258-50_12258-49delinsTA	XP_006714202.1:n.12258-50_12258-49delinsTA
XM_005262834.3:c.12258-50_12258-49delinsTA	XP_005262891.1:n.12258-50_12258-49delinsTA
XM_005262835.2:c.12258-50_12258-49delinsTA	XP_005262892.1:n.12258-50_12258-49delinsTA
XM_006714139.3:c.12258-50_12258-49delinsTA	XP_006714202.1:n.12258-50_12258-49delinsTA
NM_005245.4:c.12258-50_12258-49delinsTA MANE Select	NP_005236.2:n.12258-50_12258-49delinsTA