Canonical Allele Identifier: CA1618855296
Gene: FLOT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30742262G= , CM000668.2:g.30742262G= GRCh38
NC_000006.11:g.30710039G= , CM000668.1:g.30710039G= GRCh37
NC_000006.10:g.30818018G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376389.8:c.-14-59C= MANE Select ENSP00000365569.3:n.-14-59C=
ENST00000376389.7:c.-14-59C= ENSP00000365569.3:n.-14-59C=
ENST00000413165.5:c.-95C= ENSP00000395333.1:n.-95C=
ENST00000418160.5:c.74C= ENSP00000404300.1:p.Pro25=
ENST00000438162.5:c.-14-59C= ENSP00000400615.1:n.-14-59C=
ENST00000445853.5:c.-73C= ENSP00000398834.1:n.-73C=
ENST00000454845.1:c.-14-59C= ENSP00000391341.1:n.-14-59C=
ENST00000470643.5:n.207-59C=
ENST00000484168.1:n.181-59C=
ENST00000484693.1:n.152-59C=
NM_005803.2:c.-14-59C= NP_005794.1:n.-14-59C=
XM_005248780.3:c.-14-59C= XP_005248837.1:n.-14-59C=
XM_005248781.3:c.-14-59C= XP_005248838.1:n.-14-59C=
XM_006714947.2:c.-14-59C= XP_006715010.1:n.-14-59C=
NM_001318875.1:c.-14-59C= NP_001305804.1:n.-14-59C=
NM_005803.3:c.-14-59C= NP_005794.1:n.-14-59C=
XM_006714947.3:c.-14-59C= XP_006715010.1:n.-14-59C=
XM_017010157.1:c.43-59C= XP_016865646.1:n.43-59C=
XM_017010158.1:c.43-59C= XP_016865647.1:n.43-59C=
NM_005803.4:c.-14-59C= MANE Select NP_005794.1:n.-14-59C=
NM_001318875.2:c.-14-59C= NP_001305804.1:n.-14-59C=