Canonical Allele Identifier: CA1618853818

Gene: FLOT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30738584T= , CM000668.2:g.30738584T=	GRCh38
NC_000006.11:g.30706361T= , CM000668.1:g.30706361T=	GRCh37
NC_000006.10:g.30814340T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005803.4:c.723+1574A= MANE Select	NP_005794.1:n.723+1574A=
ENST00000376389.8:c.723+1574A= MANE Select	ENSP00000365569.3:n.723+1574A=
NM_001318875.1:c.579+1574A=	NP_001305804.1:n.579+1574A=
NM_001318875.2:c.579+1574A=	NP_001305804.1:n.579+1574A=
NM_005803.2:c.723+1574A=	NP_005794.1:n.723+1574A=
NM_005803.3:c.723+1574A=	NP_005794.1:n.723+1574A=
ENST00000376389.7:c.723+1574A=	ENSP00000365569.3:n.723+1574A=
ENST00000413165.5:c.534+1574A=	ENSP00000395333.1:n.534+1574A=
ENST00000438162.5:c.723+1574A=	ENSP00000400615.1:n.723+1574A=
ENST00000476729.5:n.452+1574A=
ENST00000487376.5:n.424+1574A=
XM_005248780.3:c.723+1574A=	XP_005248837.1:n.723+1574A=
XM_005248781.3:c.579+1574A=	XP_005248838.1:n.579+1574A=
XM_006714947.2:c.564+1574A=	XP_006715010.1:n.564+1574A=
XM_006714947.3:c.564+1574A=	XP_006715010.1:n.564+1574A=
XM_017010157.1:c.711+1574A=	XP_016865646.1:n.711+1574A=
XM_017010158.1:c.612+1574A=	XP_016865647.1:n.612+1574A=