Canonical Allele Identifier: CA1618855352

Gene: FLOT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30742358A= , CM000668.2:g.30742358A=	GRCh38
NC_000006.11:g.30710135A= , CM000668.1:g.30710135A=	GRCh37
NC_000006.10:g.30818114A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005803.4:c.-14-155T= MANE Select	NP_005794.1:n.-14-155T=
ENST00000376389.8:c.-14-155T= MANE Select	ENSP00000365569.3:n.-14-155T=
NM_001318875.1:c.-14-155T=	NP_001305804.1:n.-14-155T=
NM_001318875.2:c.-14-155T=	NP_001305804.1:n.-14-155T=
NM_005803.2:c.-14-155T=	NP_005794.1:n.-14-155T=
NM_005803.3:c.-14-155T=	NP_005794.1:n.-14-155T=
ENST00000376389.7:c.-14-155T=	ENSP00000365569.3:n.-14-155T=
ENST00000438162.5:c.-15+26T=	ENSP00000400615.1:n.-15+26T=
ENST00000454845.1:c.-15+109T=	ENSP00000391341.1:n.-15+109T=
ENST00000470643.5:n.207-155T=
ENST00000484168.1:n.181-155T=
ENST00000484693.1:n.152-155T=
XM_005248780.3:c.-15+109T=	XP_005248837.1:n.-15+109T=
XM_005248781.3:c.-14-155T=	XP_005248838.1:n.-14-155T=
XM_006714947.2:c.-14-155T=	XP_006715010.1:n.-14-155T=
XM_006714947.3:c.-14-155T=	XP_006715010.1:n.-14-155T=
XM_017010157.1:c.42+109T=	XP_016865646.1:n.42+109T=
XM_017010158.1:c.42+109T=	XP_016865647.1:n.42+109T=