Canonical Allele Identifier: CA363165416

Gene: FLOT1

Linked Data

• MyVariant Identifiers: chr6:g.30710039G>T (hg19) ; chr6:g.30742262G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000376389.8:c.-14-59C>A MANE Select	ENSP00000365569.3:n.-14-59C>A
ENST00000376389.7:c.-14-59C>A	ENSP00000365569.3:n.-14-59C>A
ENST00000413165.5:c.-95C>A	ENSP00000395333.1:n.-95C>A
ENST00000418160.5:c.74C>A	ENSP00000404300.1:p.Pro25His
ENST00000438162.5:c.-14-59C>A	ENSP00000400615.1:n.-14-59C>A
ENST00000445853.5:c.-73C>A	ENSP00000398834.1:n.-73C>A
ENST00000454845.1:c.-14-59C>A	ENSP00000391341.1:n.-14-59C>A
ENST00000470643.5:n.207-59C>A
ENST00000484168.1:n.181-59C>A
ENST00000484693.1:n.152-59C>A
NM_005803.2:c.-14-59C>A	NP_005794.1:n.-14-59C>A
XM_005248780.3:c.-14-59C>A	XP_005248837.1:n.-14-59C>A
XM_005248781.3:c.-14-59C>A	XP_005248838.1:n.-14-59C>A
XM_006714947.2:c.-14-59C>A	XP_006715010.1:n.-14-59C>A
NM_001318875.1:c.-14-59C>A	NP_001305804.1:n.-14-59C>A
NM_005803.3:c.-14-59C>A	NP_005794.1:n.-14-59C>A
XM_006714947.3:c.-14-59C>A	XP_006715010.1:n.-14-59C>A
XM_017010157.1:c.43-59C>A	XP_016865646.1:n.43-59C>A
XM_017010158.1:c.43-59C>A	XP_016865647.1:n.43-59C>A
NM_005803.4:c.-14-59C>A MANE Select	NP_005794.1:n.-14-59C>A
NM_001318875.2:c.-14-59C>A	NP_001305804.1:n.-14-59C>A